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Updated: Feb 22, 2026

Generation of Genomic Deletions in Mammalian Cell Lines via CRISPR/Cas9
Published on: January 3, 2015
Characteristics of rare and private deletions identified in phenotypically normal individuals
Keiko Shimojima1,2, Toshiyuki Yamamoto1,2
1Institute of Medical Genetics, Tokyo Women's Medical University, Tokyo, Japan.
Abstract:
Genomic copy number variations (CNVs) identified through chromosomal microarray testing must be validated to confirm whether they are pathogenically and functionally relevant to their respective clinical features. Although larger deletions have a higher probability to be pathogenic, this is not always true. Phenotypically normal individuals showed five CNV deletions larger than 1.5 Mb. The genes related to autosomal dominant trait were absent within these CNV deletions.
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