Aug 15, 2020 · A DNA microarray is a tool used to determine whether the DNA from a particular individual contains a mutation in genes.

Your health care provider has ordered a genetic test called a microarray (MY-cro-a-ray) analysis. The test is also known as chromosomal microarray, whole genome microarray, array …

Scientists use DNA microarrays to measure the expression levels of large numbers of genes simultaneously or to genotype multiple regions of a genome. Each DNA spot contains …

Aug 20, 2025 · A microarray test is a genetic test that examines a person’s DNA to detect missing or duplicated segments. This laboratory technique provides a comprehensive overview of …

Follow-up testing for individuals with unexplained developmental delay or intellectual disability, autism spectrum disorders, or congenital anomalies with a previously normal conventional …

Understanding and diagnosing the potential causes of genetic conditions is an essential first step in optimizing an effective treatment plan. CMA is recommended for individuals thought to have …

Microarray is a technique that tests for copy number variation (deletions and duplications) across the genome. It can detect copy number variants at a high resolution; it is not a sequencing test.

Chromosomal Microarray Analysis provides comprehensive genetic testing for the most common chromosomal conditions as well as a large number of severe genetic conditions not detected …

If a person with a health condition has been previously found to have a variant of uncertain significance on CMA, testing a parent or relative is covered by Medicare.

A chromosomal microarray analysis, also called microarray or array, is a type of genetic test that looks for missing or extra portions of a chromosome. We call these “deletions” or …