GSM691567[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 1000097772.

Agilent-021850 SurePrint G3 Human CGH Microarray (Feature Number version)

(Submitter supplied) SurePrint G3 Human CGH Microarray 2x400K Arrays of this design have barcodes that begin with 16021850 or 2521850. Orientation: Features are numbered numbered Left-to-Right, Top-to-Bottom as scanned by an Agilent scanner (barcode on the left, DNA on the back surface, scanned through the glass), matching the FeatureNum output from Agilent's Feature Extraction software. The ID column represents the Agilent Feature Extraction feature number. more...