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. 2008 Jan 22;98(3):619–626. doi: 10.1038/sj.bjc.6604198

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Copyright © 2008 Cancer Research UK

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Distribution of insertion and deletion of repeat-unit mutations among all 1058 observed mutations. Approximately 40% of all mutations could be explained by a simple insertion of a single repeat-unit in one of the germline alleles. Insertion mutations were more frequently observed than deletion mutations (79 vs 21%). No obvious differences were seen between cases and controls.