CHROMOSOMAL MICROARRAY CMA 750K HIGH RESOLUTION Test
Test Name: CHROMOSOMAL MICROARRAY CMA 750K HIGH RESOLUTION Test
Components: Blood
Price: 2500.0 AED
Report Delivery: 2 weeks
Method: Affymetrix CytoScan? 750K Microarray
Test Type: Genetic Disorders
Doctor: Pediatrician, Physician, Gynecologist
Test Department: CYTOGENETICS
Pre Test Information: Duly filled Genomic Microarray Requisition Form (Form 19) is mandatory.
Test Details
The Chromosomal Microarray (CMA) 750K High Resolution Test is a genetic test that uses advanced technology to detect and analyze small genetic changes in an individual’s DNA. The test is designed to identify copy number variations (CNVs), which are changes in the number of copies of a particular DNA segment.
The CMA 750K test uses a high-density microarray platform to analyze over 750,000 genetic markers across the entire genome. This high level of resolution allows for the detection of very small CNVs, as well as the identification of CNVs in regions of the genome that were previously difficult to analyze.
The CMA 750K test is typically used in clinical settings to diagnose genetic disorders, such as developmental delays, intellectual disability, autism spectrum disorders, and congenital anomalies. It can also be used to identify genetic factors that may increase an individual’s risk for certain diseases or conditions.
Overall, the CMA 750K test provides a powerful tool for understanding the genetic basis of disease and can help inform treatment decisions and genetic counseling.
Test Name | CHROMOSOMAL MICROARRAY CMA 750K HIGH RESOLUTION Test |
---|---|
Components | |
Price | 2500.0 AED |
Sample Condition | Blood |
Report Delivery | 2 weeks |
Method | Affymetrix CytoScan? 750K Microarray |
Test type | Genetic Disorders |
Doctor | Pediatrician, Physician, Gynecologist |
Test Department: | CYTOGENETICS |
Pre Test Information | Duly filled Genomic Microarray Requisition Form (Form 19) is mandatory. |
Test Details | The Chromosomal Microarray (CMA) 750K High Resolution Test is a genetic test that uses advanced technology to detect and analyze small genetic changes in an individual’s DNA. The test is designed to identify copy number variations (CNVs), which are changes in the number of copies of a particular DNA segment.
The CMA 750K test uses a high-density microarray platform to analyze over 750,000 genetic markers across the entire genome. This high level of resolution allows for the detection of very small CNVs, as well as the identification of CNVs in regions of the genome that were previously difficult to analyze. The CMA 750K test is typically used in clinical settings to diagnose genetic disorders, such as developmental delays, intellectual disability, autism spectrum disorders, and congenital anomalies. It can also be used to identify genetic factors that may increase an individual’s risk for certain diseases or conditions. Overall, the CMA 750K test provides a powerful tool for understanding the genetic basis of disease and can help inform treatment decisions and genetic counseling. |