Pitfalls in the use of DGV for CNV interpretation

American Journal of Medical Genetics, Part A

Volumn 155, Issue 10, 2011, Pages 2593-2596

  Duclos, Aude ^a,b   Charbonnier, Françoise ^a,b   Chambon, Pascal ^a,b   Latouche, Jean Baptiste ^a,b   Blavier, André ^c   Redon, Richard ^d   Frébourg, Thierry ^a,b   Flaman, Jean Michel ^a  

^a UNIVERSITÉ DE ROUEN   (France)

^b ROUEN UNIVERSITY HOSPITAL   (France)

^c Interactive Biosoftware   (France)

^d INSERM   (France)

Author keywords

[No Author keywords available]

Indexed keywords

ALLELIC IMBALANCE; ARTICLE; BIOINFORMATICS; COMPARATIVE GENOMIC HYBRIDIZATION; COPY NUMBER VARIATION; DATABASE OF GENOMIC VARIANT; DNA MICROARRAY; GENE FUNCTION; GENE IDENTIFICATION; GENE LOCATION; GENE MAPPING; GENETIC DATABASE; GENETIC POLYMORPHISM; GENOME ANALYSIS; GENOME SIZE; GENOTYPE; HEREDITARY NONPOLYPOSIS COLORECTAL CANCER; HUMAN; IMMUNE SYSTEM; IMMUNOME DATABASE; MEDICAL GENETICS; MULTIPLEX POLYMERASE CHAIN REACTION; PRIORITY JOURNAL; SENSITIVITY AND SPECIFICITY; TANDEM REPEAT; WEB BROWSER;

COLORECTAL NEOPLASMS, HEREDITARY NONPOLYPOSIS; COMPARATIVE GENOMIC HYBRIDIZATION; DATABASES, GENETIC; DNA COPY NUMBER VARIATIONS; GENETICS, MEDICAL; GENOMIC STRUCTURAL VARIATION; HUMANS; RESEARCH DESIGN;

EID: 80053110974     PISSN: 15524825     EISSN: 15524833     Source Type: Journal    
DOI: 10.1002/ajmg.a.34195     Document Type: Article

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