Cytogenetic Testing: 2.7 M SNPs Chromosomal Microarray on Blood

Also known as: chromosomal microarray, congenital blood test, cytogenetic testing.

What is cytogenetic testing: 2.7 M SNPS chromosomal microarray on blood?

SNP’s or single nucleotide polymorphisms are single abnormalities in genes on your child’s chromosomes. Following a chromosomal analysis, microarray technology allows for millions of sites on the chromosome, plus other genetic information to be tested for abnormalities.

Approximately 10% of children with unexplained mental problems/developmental abnormalities or abnormal facial features as well as some children with congenital malformations may have gene abnormalities which can detected by microarray technology.

What happens during the procedure?

Blood is withdrawn from a vein in the usual way and then sent to the genetics laboratory for testing.

Is any special preparation needed?

No special preparation is needed for this test.

What are the risk factors?

There are minimal risks for infection, bleeding, bruising, swelling or damage to nearby structures when the blood is drawn.

Reviewed by: Jack Wolfsdorf MD.

This page was last updated on: April 08, 2024 02:51 PM

Clinical Genetics

Our clinical geneticists and genetic counselors at Nicklaus Children's Hospital evaluate children with developmental delays, unusual facial features, metabolic disorders, seizures, craniofacial anomalies and failure to thrive.

Learn More