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. 2013 Sep 17;15(12):1684–1695. doi: 10.1093/neuonc/not116

Table 2.

SF+ samples are positively corrected with CNA 7p10q, CLA and IGS-18 subtype and IDH1-WT tumors

Group
SF− SFnp SF+ P
n = 12 n = 15 n = 19
TCGA
 ND 1 2 2
 CLA 2 3 11 .0086
 MES 2 2 2
 NEU 1 2 2
 PRO 6 6 2 .0183
IGS
 ND 1 2 2
 16 0 0 1
 17 3 6 3 .296
 18 3 1 10 .0078
 22 1 0 0
 23 1 3 3
 9 3 3 0 .032
IDH
 MUT 7 6 0 .00021
 WT 5 9 19
1p19q loss
 ND 4 2 8
 Loss 4 3 0 .066
 NC 4 10 11
Chr7p10q
 ND 6 10 8
 Normal 5 4 0
 Present 1 1 11 .00022
EGFR
 ND 6 10 8
n < 4 5 3 7
n > 4 1 2 4
CDKN2A/B
 ND 6 10 8
 NC 3 3 2
n < 2 3 2 9 .18

Table illustrates an overview of the distribution of previously identified driver alterations and subtypes associated with glioma. Significance levels are derived from Fishers exact test–based comparison between SF+ vs SF−/SFnp combined cohort. Abbreviations (for group names similar to Table 1): ND, not determined; NC, no change; MES, mesenchymal; NEU, neuronal; PRO, proneural; CLA, classical. 1p19q signifies the combined loss of chromosome 1p and 19q. Chr7p10q, the combined gain of 7p and loss of 10q.