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81277 - for copy number and loss-of-heterozygosity variants for chromosomal abnormalities
This procedure appears on the selected insurer prior authorization source.
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Procedure / Servicefor copy number and loss-of-heterozygosity variants for chromosomal abnormalities
Procedure / Service Description
zygosity in multiple birth pregnancies) (List separately in addition to code for primary - 81276 variant(s) (eg, codon 61, codon 146) Cytogenomic neoplasia (genome-wide) microarray analysis, interrogation of genomic regions 81277 for copy number and loss-of-heterozygosity variants for chromosomal abnormalities IGH@/BCL2 (t(14;18)) (eg, follicular lymphoma) translocation analysis, major breakpoint 81278 region (MBR) and minor cluster region (mcr) breakpoints, qualitative or quantitative
Likely documents
- Confirm benefit details
- Submit clinical notes if requested by the plan
Next actions
- Confirm the current plan policy before submission.
- Use the insurer authorization workflow for this listed code.