#ExistRefRangeSet>
Reference Interval:
#ExistRefRange>By report
*ExistRefRange>
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*ExistRefRangeSet>
#ExistInterpDataSet>
| Interpretive Data: |
#ExistInterpData>
Refer to Statement A under Testing Information at http://www.aruplab.com.
*ExistInterpData>
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*ExistInterpDataSet>
#ExistNote>
| Note: |
Fluorescence in situ Hybridization panel is performed for CLL prognosis-specific genomic abnormalities as follows: ATM deletion, D13S319 deletion, Trisomy 12, TP53 deletion.
A processing fee will be charged if this procedure is canceled at the client's request, after the test has been set up, or if the specimen integrity is inadequate to allow culture growth
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*ExistNote>
#ExistCPT>
| CPT Code(s): |
88271 x4 DNA probe; 88275 x4 Chromosomal in situ hybridization 100-300 cells; 88291 Interpretation and report - Additional CPT code modifiers may be required for procedures performed to test for oncologic or inherited disorders
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*ExistCPT>
#ExistCrossReferences>
Cross References: |
Chromosome Analysis (Chromosome FISH, CLL Panel), Chronic Lymphocytic Leukemia (Chromosome FISH, CLL Panel) |
*ExistCrossReferences>