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    Copy number variation at 1q21.1 associated with neuroblastoma

    Copy number variations (CNVs) and single nucleotide polymorphisms (SNPs) are two important potential sources of phenotypic variation in humans. Until now, only SNPs have been associated with cancer, but the in...

    Sharon J. Diskin, Cui** Hou, Joseph T. Glessner, Edward F. Attiyeh… in Nature (2009)