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Items: 3

1.

Rare Copy Number Variation in Extremely Impulsively Violent Males

(Submitter supplied) The Illumina Human Omni2.5 array is a high resolution microarray platform for studying copy number variations in the human genome. It is widely being used in both clinical and research settings for identifying causative variants as well as interrogating the genome for benign variants. We employed this platform to investigate the risk factor CNVs in 281 individuals diagnosed with Antisocial Personality Disorder.
Organism:
Homo sapiens
Type:
Genome variation profiling by SNP array
Platforms:
GPL21135 GPL25201
281 Samples
Download data: TXT
Series
Accession:
GSE116022
ID:
200116022

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2.

IlluminaHumanOmni2.5Exome-8 v1.1 A

(Submitter supplied) see manufacturer's website
Organism:
Homo sapiens
7 Series
264 Samples
Download data: CSV
Platform
Accession:
GPL21135
ID:
100021135

3.

Genotyping data for sample 381G

Organism:
Homo sapiens
Source name:
genomic DNA from whole blood
Platform:
GPL21135
Series:
GSE116022
Download data: TXT
Sample
Accession:
GSM3207534
ID:
303207534

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db=gds|term=GSM3207534[Accession]|query=1|qty=2|blobid=MCID_674c45e0d8260840384ffe40|ismultiple=true|min_list=5|max_list=20|def_tree=20|def_list=|def_view=|url=/Taxonomy/backend/subset.cgi?|trace_url=/stat?
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