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Title: Detection of de novo and homozygous copy number variants in 99 autism simplex trios      
keywords:
Variation
ID:
PRJNA130849
description:
Comparison of whole genome exome array CGH to a commercial SNP array for detection of de novo and homozygous copy number variants in 99 autism simplex trios. Will update once manuscript is prepared. Overall design: Agilent custom designed array comparative genomic hybridization (CGH) was performed on 100 samples with a diagnosis of autism. Unaffected parents of the 100 probands were also tested. A common male reference was used for all samples and parents. Samples were obtained from the Simons Simplex Collection. Three samples (11154_P1, 11154_Mo, 11154_Fa) were removed from the final analysis for quality control.
accesstypes:
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landingpage: http://www.ncbi.nlm.nih.gov/bioproject/PRJNA130849
authentication:
none
authorization:
none
ID:
pmid:21865298
dateReleased:
04-30-2011
name:
Homo sapiens
ncbiID:
ncbitax:9606
abbreviation:
NCBI
homePage: http://www.ncbi.nlm.nih.gov
ID:
SCR:006472
name:
National Center for Biotechnology Information
homePage: http://www.ncbi.nlm.nih.gov/bioproject
ID:
SCR:004801
name:
NCBI BioProject
  • HD-37283/HD/NICHD NIH HHS/United States

  • R01 HD037283-13/HD/NICHD NIH HHS/United States

  • R01 HD037283-11A2/HD/NICHD NIH HHS/United States

  • HG-4009/HG/NHGRI NIH HHS/United States

  • R01 HD037283-12/HD/NICHD NIH HHS/United States

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