GEO series

Structural Variation of Chromosomes in Autism Spectrum Disorder.

GSE9222 Homo sapiens Genome variation profiling by SNP array; SNP genotyping by SNP array 1318 samples Submitted 2007/12/20 Platform GPL3811Platform GPL3720Platform GPL3812Platform GPL3718

Summary

Chromosomal abnormalities have been identified in some individuals with Autism Spectrum Disorder (ASD), but their full etiologic role is unknown. Submicroscopic copy number variation (CNV) represents a considerable source of genetic variation in the human genome that contributes to phenotypic differences and disease susceptibility. To explore the contribution CNV imbalances in ASD, we genotyped unrelated ASD index cases using the Affymetrix GeneChip® 500K single nucleotide polymorphism (SNP) mapping array. Keywords: Whole Genome Mapping SNP Genotyping Array

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Direct links to NCBI, no account and no request form: the whole study as GSE9222_RAW.tar, processed values as the series matrix, the supplementary file directory, and per-sample supplementary files for any of the 1318 samples.

Whole study · RAW.tar ↓ Series matrix ↓ All supplementary files ↗

Also filed as BioProject PRJNA102819. Searching any of these in the dataset finder brings you back here.

NCBI GEO page ↗ Paper (PMID 18252227) ↗

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