GSM691564[Accession] - GEO DataSets

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Items: 3

Select item 2000279651.

CNVs in spermatogenic failure

(Submitter supplied) To determine the involvement of Copy Number Variants (CNVs) in the origin of male infertility, patients with idiopathic severe oligozoospermia, Sertoli-cell-only syndrome and controls with normozoospermia were analysed by array CGH using the 244A/400K array sets (Agilent Technologies).

Organism:: Homo sapiens

Type:: Genome variation profiling by genome tiling array

Platforms:: GPL9777 GPL4091
46 Samples

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Accession:: GSE27965

ID:: 200027965

PubMed Full text in PMC Similar studies Analyze with GEO2R

Select item 1000040912.

Agilent-014693 Human Genome CGH Microarray 244A (Feature number version)

(Submitter supplied) This microarray is Agilent’s premium product for human DNA copy-number profiling. Over 236,000 60-mer oligonucleotide probes, specifically optimized for copy-number measurement, span coding and non-coding genomic sequences with median spacing of 7.4 kb and 16.5 kb respectively. This microarray is designed for use with Agilent’s optimized assay protocols, enabling researchers to use nanogram levels of total genomic DNA without complexity reduction. more...