Search or choose
Find the right test or package.
Chromosomal Microarray - CMA
The Chromosomal Microarray - CMA test is a high-resolution, whole-genome chromosomal microarray test that detects submicroscopic chromosomal deletions/duplications, known as copy number variants (CNVs), which are associated with various genetic disorders.
Chro...
DiagnosticsLab test
Know more about this test
The Chromosomal Microarray - CMA test is a high-resolution, whole-genome chromosomal microarray test that detects submicroscopic chromosomal deletions/duplications, known as copy number variants (CNVs), which are associated with various genetic disor...
Understanding Chromosomal Microarray - CMA
According to American College of Medical Genetics and Genomics (ACMG) Microarray methodologies, including array comparative genomic hybridization and single nucleotide polymorphism (SNP) detecting arrays, are accepted as an appropriate first-tier test for the evaluation of imbalances associated with intellectual disability, autism, and multiple congenital anomalies. Chromosomal microarray (CMA) is a sophisticated microarray technology that analyzes the entire genome, detecting submicroscopic chromosomal deletions/d...
What does Chromosomal Microarray - CMA measure?
Chromosomal Microarray - CMA includes Chromosomal Microarray - CMA.
Related parameters
How does home sample collection work?
Select slot
Pick a convenient time.
Phlebotomist visit
A trained expert arrives home.
Safe testing
Samples move through the lab process.
Digital reports
Reports are delivered online.