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Affymetrix SNP6.0 on Ollier disease-related tumors

ABSTRACT: Mutations in the PTH1R gene were reported but these mutations are limited to a small subgroup of patients. The etiology of Ollier disease is unknown. We therefore undertook genome-wide copy number and loss of heterozygosity (LOH) analysis using Affymetrix SNP 6.0 arrays on 37 tumors of 28 Ollier patients in combination with expression array using Illumina Beadarray v3.0 for 7 tumors of 6 patients. We used Affymetrix SNP 6.0 to find out LOH and copy number alterations in Ollier tumors.

ORGANISM(S): Homo sapiens

PROVIDER: GSE22984 | GEO | 2011/08/26

SECONDARY ACCESSION(S): PRJNA129151

REPOSITORIES: GEO

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Affymetrix SNP6.0 on Ollier disease-related tumors

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