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Copy-number variation (CNV) constitutes a large proportion of total genomic variation and is increasingly recognized to be an extremely important risk factor for cancer. To examine the role of CNVs in glioblastoma, a genome-wide association study of CNVs in glioblastoma was conducted by assaying 221 tumor tissues and 28 normal tissues samples from primary glioblastoma multiform patients in TCGA project...
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