Additional file 3 of A comprehensive DNA panel next generation sequencing approach supporting diagnostics and therapy prediction in neurooncology

Additional file 3: Supplementary Table 3. Tabular survey of all panel sequencing results. Validation cases and clinically requested cases are indicated, also the 17 cases that were used for intensified quality control (QC cohort). HOMDEL: homozygous loss, HIGHCOPY: highcopy amplification, TRU: truncating variation probably leading to a loss of function, MUT: somatic missense variations, LOH: loss of heterozygosity, DEL: deletion, AMP: amplification, MUTGER: germline SNP with minor allele frequency European (non-Finnish) < 0.01 and number of homozygotes SNPs < 5, DELp/AMPp/LOHp: partial variation of a chromosomal arm.