Chromosomal Microarray tests in Dubai & UAE

Compare available Chromosomal Microarray tests, their listed prices and the information provided for each option. Test selection and preparation should be discussed with your clinician.

Tests in this category

Listed price range

1,800.00–4,000.00 AED

Clinical preparation

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Chromosomal Microarray test prices

Showing 1–9 of 9 matching tests.

Chromosomal Microarray diagnostic tests, details, and listed prices
Test and description	Specimen	Typical duration	Price	Options
TEST-612 Chromofic KaryoArray™ Test This diagnostic test evaluates chromosomal copy number variations (CNVs), loss of heterozygosity (LOH), and updates (UPD) using a high-resolution microarray and microscopy.	Whole Blood (EDTA & Sodium Heparin)	10 working days	4,000.00 AED	View
View test specifications and preparation Hide test specifications and preparation What it measures ["Copy Number Variations (CNVs)", "Loss of Heterozygosity (LOH)", "Updates of Dominance (UPD)", "Mosaicism"] Parameters [] Preparation ["No special preparation required", "Keep the patient well-hydrated", "Inform the phlebotomist of any bleeding disorders or anticoagulant use"] Indications ["Diagnosis of genetic causes for neurodevelopmental disorders", "Evaluation of congenital anomalies", "Assessment of developmental delay or intellectual disability", "Detection of submicroscopic chromosomal imbalances"] Measurement technique Confirm with laboratory Codes LOINC: 81273-3 ICD-10: F88 Clinical summary This diagnostic test evaluates chromosomal copy number variations (CNVs), loss of heterozygosity (LOH), and updates (UPD) using a high-resolution microarray and microscopy.
TEST-607 Chromosomal Microarray (CMA) 750K High Resolution Test This test evaluates the entire genome for clinically significant copy number variations (CNVs), including microdeletions and microduplications.	Peripheral Whole Blood (EDTA tube)	15 Working Days	2,800.00 AED	View
View test specifications and preparation Hide test specifications and preparation What it measures ["Copy Number Variations (CNVs)", "Single Nucleotide Polymorphisms (SNPs)"] Parameters [] Preparation ["No fasting or special preparation is needed.", "Ensure the Genomic Microarray Requisition Form (Form 19) is fully completed and signed by your ordering physician."] Indications ["Unexplained developmental delay or intellectual disability", "Autism spectrum disorder", "Multiple congenital anomalies", "Prenatal genetic screening", "Recurrent pregnancy loss"] Measurement technique Confirm with laboratory Codes LOINC: 81200-8 ICD-10: Z13.71, Z01.818 Clinical summary This test evaluates the entire genome for clinically significant copy number variations (CNVs), including microdeletions and microduplications.
TEST-1364 Chromosomal Microarray 180K (CMA 180K) Test This test detects submicroscopic deletions and duplications across all chromosomes using a CGH+SNP microarray platform.	Amniotic Fluid / CVS / Cord Blood / Products of Conception (POC) / Peripheral Blood	7–9 working days	3,800.00 AED	View
View test specifications and preparation Hide test specifications and preparation What it measures ["Copy Number Variations (CNVs)", "Submicroscopic deletions", "Submicroscopic duplications"] Parameters [] Preparation [] Indications ["Prenatal diagnosis with ultrasound anomalies", "Unexplained developmental delay or intellectual disability", "Stillbirth evaluation", "Recurrent pregnancy loss evaluation", "Pre-implantation genetic screening"] Measurement technique Confirm with laboratory Codes LOINC: 93720-5 ICD-10: Z31.5, O36.4, R62.50 Clinical summary This test detects submicroscopic deletions and duplications across all chromosomes using a CGH+SNP microarray platform.
TEST-1370 Chromosomal Microarray 315K (AF/CVS/CB/POC/PB) Test This diagnostic test evaluates the entire genome for clinically significant copy number variations (CNVs), including microdeletions and microduplications, using a high-resolution m...	Amniotic Fluid, Chorionic Villus Sampling (CVS), Cord Blood, Products of Conception (POC), Peripheral Blood	7–9 working days	2,200.00 AED	View
View test specifications and preparation Hide test specifications and preparation What it measures ["Copy Number Variants (CNVs)", "Regions of Homozygosity (LOH)", "Mosaic Abnormalities"] Parameters [] Preparation ["No specific patient preparation is required.", "Do not discontinue prescribed medication without consulting your physician."] Indications ["Confirmation of fetal anomalies", "Investigation of stillbirth", "Evaluation of recurrent pregnancy loss", "Diagnosis of suspected microdeletion syndromes", "Assessment of developmental delay or intellectual disability"] Measurement technique Confirm with laboratory Codes LOINC: 82121-8 ICD-10: Z31.5 Clinical summary This diagnostic test evaluates the entire genome for clinically significant copy number variations (CNVs), including microdeletions and microduplications, using a high-resolution microarray.
TEST-1362 Chromosomal Microarray 60K (Amniotic Fluid/CVS/Cord Blood) Test This test evaluates fetal chromosomes for copy number variations (CNVs), including microdeletions and microduplications, using a high-density microarray.	Amniotic fluid, Chorionic villus sample (CVS), or Cord blood	7–9 business days	2,600.00 AED	View
View test specifications and preparation Hide test specifications and preparation What it measures ["Copy Number Variations (CNVs)", "Microdeletions", "Microduplications", "Uniparental Disomy (UPD)", "Mosaicism"] Parameters [] Preparation [] Indications ["Fetal structural anomalies", "Abnormal ultrasound findings", "Family history of genetic conditions", "Advanced maternal age"] Measurement technique Confirm with laboratory Codes LOINC: 92833-4 ICD-10: O28.5, Z36 Clinical summary This test evaluates fetal chromosomes for copy number variations (CNVs), including microdeletions and microduplications, using a high-density microarray.
TEST-1348 Chromosomal Microarray 60K (Products of Conception) Test This test evaluates fetal tissue for chromosomal abnormalities, including deletions, duplications, and copy number variants (CNVs), using microarray technology.	Products of Conception Tissue (Sterile Saline/RPMI) + Optional Maternal EDTA Blood	15–20 Days	1,800.00 AED	View
View test specifications and preparation Hide test specifications and preparation What it measures ["Chromosomal deletions", "Chromosomal duplications", "Copy Number Variants (CNVs)", "Absence of Heterozygosity (AOH)", "Mosaicism", "Triploidy"] Parameters [] Preparation ["Collect Products of Conception tissue in sterile saline or RPMI medium.", "Transport sample at 2–8°C.", "Optional maternal EDTA blood may be drawn concurrently."] Indications ["Investigation of pregnancy loss", "Recurrent pregnancy loss", "Identification of genetic causes of fetal abnormalities"] Measurement technique Confirm with laboratory Codes LOINC: 62356-1 ICD-10: O02.1, N96, Z13.79 Clinical summary This test evaluates fetal tissue for chromosomal abnormalities, including deletions, duplications, and copy number variants (CNVs), using microarray technology.
TEST-642 Chromosomal Microarray Optima Prenatal Test This test evaluates the fetus for chromosomal copy number variations (deletions and duplications) across the entire genome.	Amniotic fluid, chorionic villus, cord blood	10 working days	2,500.00 AED	View
View test specifications and preparation Hide test specifications and preparation What it measures ["Genome-wide copy number variations", "Chromosomal deletions", "Chromosomal duplications"] Parameters [] Preparation [] Indications ["Abnormal ultrasound findings", "Advanced maternal age", "Family history of known genetic disorders"] Measurement technique Confirm with laboratory Codes LOINC: 93719-0 ICD-10: Z36.8, O28.9 Clinical summary This test evaluates the fetus for chromosomal copy number variations (deletions and duplications) across the entire genome.
TEST-641 Chromosomal SNP Microarray for Products of Conception (POC) Testing Test This diagnostic test evaluates products of conception tissue for chromosomal abnormalities, including copy number variants, uniparental disomy, and triploidy.	Products of Conception (POC) Tissue	10 working days	2,500.00 AED	View
View test specifications and preparation Hide test specifications and preparation What it measures ["Copy Number Variants (CNVs)", "Uniparental Disomy (UPD)", "Triploidy", "Microdeletions"] Parameters [] Preparation ["Provide 5 mg (minimum 2 mg) of products of conception tissue collected in sterile normal saline.", "Complete the mandatory Genomic Microarray Requisition Form 19."] Indications ["Investigation of miscarriage tissue", "Recurrent pregnancy loss", "Evaluation of potential genetic causes for pregnancy failure"] Measurement technique Confirm with laboratory Codes LOINC: 82125-4 ICD-10: O36.80 Clinical summary This diagnostic test evaluates products of conception tissue for chromosomal abnormalities, including copy number variants, uniparental disomy, and triploidy.
TEST-1353 Microarray 750K Chromosomal Analysis (AF/CVS/CB/POC/PB) Test This test evaluates the entire genome for copy number variations and loss of heterozygosity using a high-density SNP microarray.	Amniotic Fluid, Chorionic Villi, Cord Blood, Peripheral Blood, Products of Conception	7–9 working days	2,500.00 AED	View
View test specifications and preparation Hide test specifications and preparation What it measures ["Copy Number Variations (CNVs)", "Loss of Heterozygosity (LOH)", "Genome-wide scanning"] Parameters [] Preparation ["No specific patient preparation is required.", "Ensure sample collection is performed within an accredited hospital facility."] Indications ["Prenatal screening for chromosomal abnormalities", "Investigation of developmental delay or intellectual disability", "Evaluation of multiple congenital anomalies", "Diagnosis of suspected genetic syndromes", "Assessment of unexplained infertility or recurrent pregnancy loss"] Measurement technique Confirm with laboratory Codes LOINC: 82164-0 ICD-10: Z13.79 Clinical summary This test evaluates the entire genome for copy number variations and loss of heterozygosity using a high-density SNP microarray.

Category overview

Chromosomal Microarray: overview

When a child presents with unexplained autism, developmental delays, or congenital anomalies, a standard chromosomal test may not be enough to find the tiny, hidden genetic culprits. As the gold standard for high-resolution genomic testing within our Genetics department, the Chromosomal Microarray (CMA) deeply scans the entire genome to detect microscopic deletions or duplications of DNA that traditional karyotyping misses. By leveraging state-of-the-art molecular technology, this critical diagnostic screening ends the diagnostic odyssey, providing the definitive data needed to safely guide specialized pediatric neurology care, early behavioral interventions, and tailored educational support. Trusted for advanced genomic excellence among premier diagnostic labs in Dubai and the UAE, DNA Labs guarantees absolute patient confidentiality, uncompromising analytical precision, and rapid, dependable reporting. Support your child’s developmental potential—book your chromosomal microarray testing in UAE, arrange a secure clinical sample collection, or connect with our specialized genetic counselors today.

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Use the test details as a conversation starter

The right diagnostic option depends on your reason for testing and individual circumstances. Check the listed specimen and timing, then confirm any preparation requirements with the ordering clinician or laboratory before collection.