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81349 - Cytogenomic (genome-wide) analysis for constitutional chromosomal abnormalities

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Procedure / ServiceCytogenomic (genome-wide) analysis for constitutional chromosomal abnormalities
Procedure / Service Description

Genetic and Molecular Testing Medical Necessity Guideline - 81348 SRSF2 (serine and arginine-rich splicing factor 2) (eg, myelodysplastic syndrome, acute myeloid leukemia) gene analysis, common variants (eg, P95H, P95L) 81349 Cytogenomic (genome-wide) analysis for constitutional chromosomal abnormalities; interrogation of genomic regions for copy number and loss-of-heterozygosity variants, low-pass sequencing analysis

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  • Submit clinical notes if requested by the plan
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