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Table 2 CNVs and mutations in molecular groups of CNS-PNET

From: Molecular analysis of pediatric CNS-PNET revealed nosologic heterogeneity and potent diagnostic markers for CNS neuroblastoma with FOXR2-activation

Molecular alterations

CNS_NBL (20)

GBM_G34 (22)

GBM_MYCN (18)

EPN_RELA (24)

MYCN amplifications

0

0

70%

0

PDGFRA amplification

0

30%

0

0

CCND2 amplification

0

20%

0

0

1q gain

100%

40%

50%

30%

2p gain

20%

10%

70%

10%

3p loss

60%

10%

10%

0

3q loss

0

70%

10%

0

4q loss

10%

70%

10%

10%

6q loss

40%

0

5%

10%

9p loss

0

40%

10%

45%

10q loss

30%

70%

50%

30%

16q loss

70%

20%

10%

0

17p loss

0

10%

50%

0

17q gain

60%

30%

5%

5%

22q loss

0

15%

15%

30%

Recurrent mutations

No

G34V/R—22/22

TP53—13/18

No

Recurrent fusions (54)

FOXR2—14/14

No

NBAS—3/12

RELA—20/20