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. 2021 Sep 15;24(10):103132. doi: 10.1016/j.isci.2021.103132

Table 2.

Pediatric tumors classified by alteration frequencies, classical translocations and deletions, in comparison with adult NSLC

Tumor type Alterations/Mb Classical alterations
ATRT/MRT ∼3/whole exome
<1 per Mb exome (Grobner et al., 2018)
del(22q11.23)
SNF5/SMARCB1
Myeloid leukemias <1 per Mb exome
0.6 per Mb exome (Grobner et al., 2018)
t(11q23) MLL-rearr.
t(8; 21) AML-ETO
inv(16) CBFb-MYH11
Ewing sarcoma <1 per Mb exome
0.6 per Mb exome (Grobner et al., 2018)
(11; 22) (q24; q12)
EWS-FLI-1
Diffuse Intrinsic Pontine Glioma 1.2 per Mb exome (Grobner et al., 2018) H3.3K27M
H3.1K27M
Synovial sarcoma 1.7 per Mb exome (Chalmers et al., 2017) t(X; 18)
SS18-SSX
Rhabdomyosarcoma 1.7 per Mb exome∗ (alveolar)
2.5 per Mb exome (Chalmers et al., 2017)
(embryonal)
1.3 per Mb exome (Grobner et al., 2018) (embryonal)
t(2; 13) (q35; q14)
PAX3-FOXO1
MPNST 2.5 per Mb exome (Chalmers et al., 2017) del(17q11) NF1▵; SUZ12▵
del(11q14) EED▵
NSCLC 8.1 per Mb exome (Chalmers et al., 2017) SMARCA4 mutations
19p13.2
Osteosarcoma 14.6 per Mb exome (CNV) (Poos et al., 2015; Kovac et al., 2015)
1.8 per Mb exome (SNV)
1.3 per Mb exome (SNV)
(Grobner et al., 2018)
Complex karyotype/hyperdiploidy
−10, -19
+4q, +8q, +17p

The class of (✧) pediatric tumor and (▵) adult tumor are defined, as well as classical alterations, mutational burden per exome, and relevant pioneer factor.