Table 2 Numbers of genetic aberrations observed per case.

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

Case ID

Histopathological growth patterns

Nonsynonymous somatic SNV & indels

DEL

INV

DUP

BND

1

NLPHL C/E

263

0

5

0

12

2

NLPHL pattern E

26

0

0

0

3

3

NLPHL pattern E

843

491

32

43

24

4

NLPHL C/E

209

96

193

13

Not applicablea

5

THRLBCL

247

49

11

2

8

6

THRLBCL

4527

30

13

5

46

7

NLPHL pattern E

58

5

8

2

4

  1. SNV single nucleotide variants, DEL deletions, INV inversions, DUP duplications, BND break-ends.
  2. aDue to the presence of contaminating vector sequences, genome-wide calling of break-ends was not reliable for case 4.
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