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Copy number variation

Analysis of copy number loss of the ErbB4 receptor tyrosine kinase in glioblastoma

DeAnalisa C. Jones, Adriana Scanteianu, [ ... ], Marc R. Birtwistle

aCNViewer: Comprehensive genome-wide visualization of absolute copy number and copy neutral variations

Victor Renault, Jörg Tost, [ ... ], Alexandre How-Kit

Copy number variation analysis in cytochromes and glutathione S-transferases may predict efficacy of tyrosine kinase inhibitors in chronic myeloid leukemia

Alexander V. Lavrov, Oksana A. Ustaeva, [ ... ], Sergey I. Kutsev

Whole-genome sequencing reveals mutational landscape underlying phenotypic differences between two widespread Chinese cattle breeds

Yao Xu, Yu Jiang, [ ... ], Hong Chen

Highly dynamic temporal changes of TSPY gene copy number in aging bulls

Olutobi A. Oluwole, Kiana Mahboubi, [ ... ], William Allan King

Copy number variation of FCGR genes in etiopathogenesis of sarcoidosis

Marlena Typiak, Krzysztof Rębała, [ ... ], Anna Dubaniewicz

A new GTF2I-BRAF fusion mediating MAPK pathway activation in pilocytic astrocytoma

Tajana Tešan Tomić, Josefin Olausson, [ ... ], Frida Abel

Embryonic loss of human females with partial trisomy 19 identifies region critical for the single active X

Barbara R. Migeon, Michael A. Beer, Hans T. Bjornsson

Diversification of spatiotemporal expression and copy number variation of the echinoid hbox12/pmar1/micro1 multigene family

Vincenzo Cavalieri, Fabiana Geraci, Giovanni Spinelli

Novel copy number variation of the TGFβ3 gene is associated with TGFβ3 gene expression and duration of fertility traits in hens

Lantao Gu, Chenghao Sun, [ ... ], Shijun Li

Confirmation of the OVOL2 Promoter Mutation c.-307T>C in Posterior Polymorphous Corneal Dystrophy 1

Doug D. Chung, Ricardo F. Frausto, [ ... ], Anthony J. Aldave

Rare CNVs in Suicide Attempt include Schizophrenia-Associated Loci and Neurodevelopmental Genes: A Pilot Genome-Wide and Family-Based Study

Marcus Sokolowski, Jerzy Wasserman, Danuta Wasserman

Chromosomal Instability Estimation Based on Next Generation Sequencing and Single Cell Genome Wide Copy Number Variation Analysis

Stephanie B. Greene, Angel E. Dago, [ ... ], Mark Landers

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