EGAD00010000466

Down syndrome CNV genotyping data

27/05/2015
108 samples
DAC: EGAC01000000023
Technology: NimbleGen 135K aCGH - NimbleScan

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Studies are experimental investigations of a particular phenomenon, e.g., case-control studies on a particular trait or cancer research projects reporting matching cancer normal genomes from patients.

Study ID	Study Title	Study Type
	The complex SNP and CNV genetic architecture of the increased risk of congenital heart defects in Down syndrome	Other

This table displays only public information pertaining to the files in the dataset. If you wish to access this dataset, please submit a request. If you already have access to these data files, please consult the download documentation.

ID	File Type	Size
EGAF00000199711	txt	1.9 kB
EGAF00000199712	txt	1.0 MB
2 Files (1.1 MB)