Fig. 2: Somatic SNV and InDel mutations and genomic aberrations in the seven cases of NLPHL/THRLBCL. | Leukemia

Fig. 2: Somatic SNV and InDel mutations and genomic aberrations in the seven cases of NLPHL/THRLBCL.

From: Genetic lesions in nodular lymphocyte-predominant Hodgkin lymphoma and T cell/histiocyte-rich large B-cell lymphoma identified by whole genome sequencing

Fig. 2

A Non-synonymous single nucleotide variants (SNVs) and Indels and distribution of SNV types (missense mutations, stop-gain mutations, other mutations including splice site mutations and frameshift mutations) listed by frequency (number of cases, number of variants per case). B Structural variants (SVs) per case with del: deletion-type rearrangements, dup: duplication-type rearrangements, inv: inversion-type rearrangements and bnd: inter-chromosomal rearrangements. Case 4 was excluded from this figure due to the contaminating vector sequences. C Circos plot of SVs and copy-number profile for case 3. From outside to inside, the tracks are: chromosome ideogram, read-depth, large (>10 Kbp) SVs, and inter-chromosomal rearrangements. Color scale is the same as in (B).

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