Test Overview
Chromosomal Microarray
Diagnosis of congenital copy number changes in products of conception, including aneuploidy (ie, trisomy or monosomy) and structural abnormalities. Diagnosing chromosomal causes for fetal death
Determining recurrence risk of future pregnancy losses. Determining the size, precise breakpoints, gene content, and any unappreciated complexity of abnormalities detected previously by other methods such as conventional chromosome and fluorescence in situ hybridization (FISH) studies
Determining if apparently balanced abnormalities identified by previous conventional chromosome studies have cryptic imbalances, since a proportion of such rearrangements that appear balanced at the resolution of a chromosome study are actually unbalanced when analyzed by higher-resolution chromosomal microarray
Interpretive report provided
* Reference ranges may change over time. Please refer to the original patient report when evaluating results.
Test Details
21 - 30 days
- CMA
- CMA
Specimen Requirements
A reason for referral and pathology report are required in order for testing to be performed. Send information with specimen. Acceptable pathology reports include working drafts, preliminary pathology or surgical pathology reports. Send the report along with the block OR slides
Additional Information
Test performed by Mayo Clinic Laboratories