Genomic regions and putative target genes associated with 2yDFS in NSGCT patients.

Chr: chromosomal location of copy number alteration associated with outcomeRegion: chromosomal region associated with outcomeNo.: number of tumors that display the copy number alterationAlt.: copy number alteration type (gain or loss)p-value: p-value of the association between copy number alteration and outcomeOR: odds ratio for the event95% C.I.: 95% confidence interval of the odds ratioSig. Gene: number of significantly differentially expressed genes that map to regionFDR: false discovery rate of significant genes mapping to regionGenomic regions and putative target genes associated with 2yDFS in NSGCT patients.