SVA retrotransposon insertion-associated deletion represents a novel mutational mechanism underlying large genomic copy number changes with non-recurrent breakpoints. Homo sapiens
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下载链接：
https://www.ncbi.nlm.nih.gov/bioproject/PRJNA248281
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资源简介：
Array CGH analysis in order to determine the size of atypical NF1 deletions under investigation Overall design: 12 atypical NF1 deletions were investigated with the custom array CGH
创建时间：
2014-05-21
