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Affymetrix SNP array data for acute lymphoblastic leukemia samples

GSE9113 Homo sapiens Genome variation profiling by SNP array; SNP genotyping by SNP array 1496 samples Submitted 2009/09/02 Platform GPL2005Platform GPL3720Platform GPL3718Platform GPL2004
Summary
BCR-ABL1 lymphoblastic leukaemia is characterized by the deletion of Ikaros. The Philadelphia chromosome, encoding BCR-ABL1, is the defining lesion of chronic myelogenous leukemia (CML) and a subset of acute lymphoblastic leukemia (ALL) cases. To define oncogenic lesions that cooperate with BCR-ABL1 to induce ALL, we performed genome-wide analysis of leukemic samples from 23 CML cases and 304 ALL cases, including 43 BCR-ABL1 B-ALL cases. IKZF1 (encoding the transcription factor Ikaros) was deleted in 83.7% of BCR-ABL1 B-ALL cases, but not in chronic phase CML. Deletion of IKZF1 was also identified as an acquired lesion in lymphoid blast crisis of CML. The IKZF1 deletions resulted in haploinsufficiency, expression of a dominant negative Ikaros isoform or the complete loss of Ikaros expression. Sequencing of IKZF1 deletion breakpoints suggested that aberrant V(D)J recombination is responsible for the deletions. These findings suggest that genetic lesions resulting in the loss of Ikaros function are a key event in the development of BCR-ABL1 ALL. *** Due to privacy concerns, the primary SNP array data is no longer available with unrestricted access. Individuals wishing to obtain this data for research purposes may request access using the Web links below. *** This SuperSeries is composed of the SubSeries listed below.
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Direct links to NCBI, no account and no request form: the whole study as GSE9113_RAW.tar, processed values as the series matrix, the supplementary file directory, and per-sample supplementary files for any of the 1496 samples.

Also filed as BioProject PRJNA102641. Searching any of these in the dataset finder brings you back here.

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