Genomics

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SVA retrotransposon insertion-associated deletion represents a novel mutational mechanism underlying large genomic copy number changes with non-recurrent breakpoints

ABSTRACT: Array CGH analysis in order to determine the size of atypical NF1 deletions under investigation

ORGANISM(S): Homo sapiens

PROVIDER: GSE57859 | GEO | 2014/05/29

SECONDARY ACCESSION(S): PRJNA248281

REPOSITORIES: GEO

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