Results of meta-analysis for CCL3L1 CNV and HIV-1 susceptibility.
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aNumber of comparisons.
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2010-12-30
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Table S1 - Assessing the Impact of Copy Number Variants on miRNA Genes in Autism by Monte Carlo Simulation
The APL dataset of de novo CNVs and the overlapping miRNA genes. (PDF)
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Total number of copy number alterations (CNAs) observed between the CRCs and corresponding PBTs of each pair analyzed and their respective common cytobands and range of overlap (in bold CNAs with overlap >95%).
Total number of copy number alterations (CNAs) observed between the CRCs and corresponding PBTs of each pair analyzed and their respective common cytobands and range of overlap (in bold CNAs with over
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Additional file 4 of Deep whole genome sequencing identifies recurrent genomic alterations in commonly used breast cancer cell lines and patient-derived xenograft models
Additional file 4: Table S7. Comparison of the genes with copy number alterations in COSMIC, Ben-David et al and this study.
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Uncovering obsessive-compulsive disorder risk genes in a pediatric cohort by high-resolution analysis of copy number variation.. Homo sapiens
The Affymetrix CytoScan HD 2.5M and Illumina HumanOmni2.5 arrays are high resolution SNP platform for studying copy number variations in the human genome. Both platforms have widely being used in both
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