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Germ-line DNA copy number variation frequencies in a large North American population.

Germ-line DNA copy number variation frequencies in a large North American population. Research Abstract Details 

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  • Germ-line DNA copy number variation frequencies in a large North American population. Abstract Text:

    george zogopoulosGeorge Zogopoulos,kevin c h haKevin C H Ha,faisal naqibFaisal Naqib,sara mooreSara Moore,hyeja kimHyeja Kim,alexandre montpetitAlexandre Montpetit,frederick robidouxFrederick Robidoux,philippe laflammePhilippe Laflamme,michelle cotterchioMichelle Cotterchio,celia greenwoodCelia Greenwood,stephen w schererStephen W Scherer,brent zankeBrent Zanke,thomas j hudsonThomas J Hudson,gary d baderGary D Bader,steven gallingerSteven Gallinger,george zogopoulosGeorge Zogopoulos,kevin c h haKevin C H Ha,faisal naqibFaisal Naqib,sara mooreSara Moore,hyeja kimHyeja Kim,alexandre montpetitAlexandre Montpetit,frederick robidouxFrederick Robidoux,philippe laflammePhilippe Laflamme,michelle cotterchioMichelle Cotterchio,celia greenwoodCelia Greenwood,stephen w schererStephen W Scherer,brent zankeBrent Zanke,thomas j hudsonThomas J Hudson,gary d baderGary D Bader,steven gallingerSteven Gallinger,

    Genomic copy number variation (CNV) is a recently identified form of global genetic variation in the human genome. The Affymetrix GeneChip 100 and 500 K SNP genotyping platforms were used to perform a large-scale population-based study of CNV frequency. We constructed a genomic map of 578 CNV regions, covering approximately 220 Mb (7.3%) of the human genome, identifying 183 previously unknown intervals. Copy number changes were observed to occur infrequently (<1%) in the majority (>93%) of these genomic regions, but encompass hundreds of genes and disease loci. This North American population-based map will be a useful resource for future genetic studies.

    Germ-line DNA copy number variation frequencies in a large North American population. Publishing Authors By Initials

    g zogopoulosG Zogopoulos,kc haKC Ha,f naqibF Naqib,s mooreS Moore,h kimH Kim,a montpetitA Montpetit,f robidouxF Robidoux,p laflammeP Laflamme,m cotterchioM Cotterchio,c greenwoodC Greenwood,sw schererSW Scherer,b zankeB Zanke,tj hudsonTJ Hudson,gd baderGD Bader,s gallingerS Gallinger,g zogopoulosG Zogopoulos,kc haKC Ha,f naqibF Naqib,s mooreS Moore,h kimH Kim,a montpetitA Montpetit,f robidouxF Robidoux,p laflammeP Laflamme,m cotterchioM Cotterchio,c greenwoodC Greenwood,sw schererSW Scherer,b zankeB Zanke,tj hudsonTJ Hudson,gd baderGD Bader,s gallingerS Gallinger,

    For similar abstracts research abstracts see: abstracts research

    PUBMED ID PMID:

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    Germ-line DNA copy number variation frequencies in a large North American population. Journal Published:

    PUBLICATION TYPE: Journal Article

    Journal: Human genetics

    VOLUME: 122

    Page Numbers: 345-53

    Journal Abbreviation: Hum. Genet.

    ISSN: 0340-6717

    DAY: 19

    MONTH: 07

    YEAR: 2007

    Germ-line DNA copy number variation frequencies in a large North American population. Information

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    LANGUAGE: eng

    NlmUniqueID: 7613873

    Germ-line DNA copy number variation frequencies in a large North American population. Keywords Mesh Terms:

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    Grant and Affiliation Information for Germ-line DNA copy number variation frequencies in a large North American population.

    AFFILIATION: Sam Minuk Cancer Genetics and Biomarker Laboratories, Fred Litwin Centre for Cancer Genetics, Samuel Lunenfeld Research Institute, Toronto, Canada.

    Country: Germany

    Germany Research PublicationGermany Research Publication

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    MEDLINETA: Hum Genet

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