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Diagnostic options Β· UAE

Microarray tests in Dubai & UAE

Compare available 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

2

Listed price range

3,300.00–3,600.00 AED

Clinical preparation

Confirm test-specific instructions with your clinician or laboratory.

Compare available tests

Microarray test prices

Showing 1–2 of 2 matching tests.

Microarray diagnostic tests, details, and listed prices
Test and description Specimen Typical duration Price Options
TEST-623
Chromosome XON Microarray High Resolution Test

This test evaluates the entire X chromosome for copy number variations (deletions and duplications) at a high resolution.

Peripheral Whole Blood 25 working days 3,600.00 AED
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View test specifications and preparation
What it measures
["Copy Number Variations (CNVs)", "Single Nucleotide Polymorphisms (SNPs) on X chromosome"]
Parameters
[]
Preparation
["No special preparation is required"]
Indications
["Suspected X-linked intellectual disability", "Diagnosis of developmental delay", "Investigation of congenital anomalies", "Prenatal screening (if indicated)"]
Measurement technique
Confirm with laboratory
Codes
LOINC: 82121-3 ICD-10: Q99.8, Q97.8, Q98.8
Clinical summary
This test evaluates the entire X chromosome for copy number variations (deletions and duplications) at a high resolution.
TEST-646
ChromUltra Chromosome SNP HD Microarray Test

This test evaluates the entire genome for copy number variations (CNVs), loss of heterozygosity (LOH), and single nucleotide polymorphisms (SNPs) to detect chromosomal abnormalitie...

Whole Blood (Peripheral) 15 Working Days 3,300.00 AED
View
View test specifications and preparation
What it measures
["Copy Number Variations (CNVs)", "Loss of Heterozygosity (LOH)", "Single Nucleotide Polymorphisms (SNPs)", "Chromosomal microdeletions", "Chromosomal duplications", "Regions of homozygosity"]
Parameters
[]
Preparation
["Fasting is not required", "Ensure mandatory Genomic Microarray Requisition Form 19 is completed", "Inform phlebotomy team of all current medications, especially anticoagulants or antiplatelet agents"]
Indications
["Evaluation of developmental delay or intellectual disability", "Investigation of multiple congenital anomalies", "Diagnosis of autism spectrum disorders", "Assessment of unexplained recurrent miscarriages", "Prenatal screening for chromosomal abnormalities"]
Measurement technique
Confirm with laboratory
Codes
LOINC: 92818-1 ICD-10: Z13.79
Clinical summary
This test evaluates the entire genome for copy number variations (CNVs), loss of heterozygosity (LOH), and single nucleotide polymorphisms (SNPs) to detect chromosomal abnormalities.

Category overview

Microarray: overview

When standard genetic tests leave questions unanswered, zooming in on your DNA at a microscopic level provides the definitive clarity you deserve. Representing the pinnacle of our advanced Molecular Genetics department, Chromosomal Microarray testing scans your entire genome for minute missing or duplicated DNA segments. By leveraging cutting-edge diagnostic technology, this high-resolution genetic profiling helps uncover subtle imbalances linked to developmental or neurological conditions, safely guiding highly tailored medical oversight and early interventions. Consistently trusted for complex molecular diagnostics among diagnostic labs in Dubai and the UAE, DNA Labs ensures strict patient confidentiality, unparalleled diagnostic accuracy, and prompt reporting for sensitive cases. Secure the highest level of genetic insightβ€”book your microarray testing in UAE, coordinate a secure sample collection, or consult our dedicated medical genetics experts today.

Before booking

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.