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81422 Fetal chrmoml microdeltj

Pathology & Lab

Also known as: prenatal microarray test, fetal copy number variation testing

Genetic testing for fetal chromosomal microdeletion and microduplication abnormalities using cell-free DNA analysis.

Clinical Context

Prenatal detection of submicroscopic chromosomal deletions and duplications; identifies DiGeorge syndrome, Prader-Willi, and other microdeletion syndromes.

RVU Breakdown

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Specialties

obstetricsmaternal-fetal medicinegenetics

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CPT® is a registered trademark of the American Medical Association. Data sourced from CMS Physician Fee Schedule RVU26A. Descriptions, synonyms, and clinical context are original content by RVU Edge.