Fig. 2: Copy number variants (CNVs) in EBV + DLBCL (NOS) identified through whole-genome sequencing. | Blood Cancer Journal

Fig. 2: Copy number variants (CNVs) in EBV + DLBCL (NOS) identified through whole-genome sequencing.

From: Genomic insights into the pathogenesis of Epstein–Barr virus-associated diffuse large B-cell lymphoma by whole-genome and targeted amplicon sequencing

Fig. 2

Panel (A) depicts whole genomic CNAs, whereas panel (B) illustrates the recurrent 6q losses subsequently validated by FISH (A20 in spectrum orange, PRDM1 in spectrum green) with panel displaying a wild-type constellation (C) and panel showing a case with a deletion of the A20 and PRDM1 gene locus in 6q (D).

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