Ann Lab Med.  2018 Nov;38(6):619-622. 10.3343/alm.2018.38.6.619.

Characterizing Atypical BCL6 Signal Patterns Detected by Digital Fluorescence In Situ Hybridization (FISH) Analysis

Affiliations
  • 1ARUP Institute for Clinical and Experimental Pathology, Salt Lake City, UT, USA. liewm@aruplab.com
  • 2Department of Pathology, University of Utah School of Medicine, Salt Lake City, UT, USA.
  • 3Department of Pediatrics, University of Utah School of Medicine, Salt Lake City, UT, USA.

Abstract

No abstract available.


MeSH Terms

Fluorescence*
In Situ Hybridization*

Figure

  • Fig. 1 Results from the combined testing of sample 1U. (A) Next generation sequencing identified a BCL6-IGH fusion. (B) Representative cells with 1F/1G and 2F/1G signal patterns with the BCL6 probe set. (C) The molecular inversion probe array analysis detected a copy number gain from 3p14.2 to 3q27.3.


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