This FAIRsharing record describes: Clinical information about tumor samples and microarray data, with emphasis on array comparative genomic hybridization (aCGH) and data mining of gene copy number ch
Additional file 2: Tables S1. Summary statistics for CNVs in ARS-UCD1.2 and UMD3.1. Table S2. Detailed features of CNVRs on autosomes identified in this study. Table S3. Chromosome-wide CNVR coverage
Using normalized read depth analysis to assess gene copy number variation in the PH8 strain, we identified 205 genes presenting a somy greater than 1.8. Among these genes that were considered super
DNA samples of haploid ES cells and control DNA were compared to genomic DNA of the C57B/6 inbred mouse strain on a NimbleGen Mouse CGH 3x720K Whole-Genome Tiling Array (Build MM9), (GPL10989) DNA sam
Genomic characterization of rare histological subtype of glioblastoma with giant cell features. This study evaluated copy number imbalances and copy-neutral loss of heterozygosity across a series of 1
