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Accession: PRJNA170386 ID: 170386

Homo sapiens (human)

SNP array for CNV calling AUTS2 project [Illumina]

See Genome Information for Homo sapiens
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This project is a component of the AUTS2 project
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4 additional projects are components of the AUTS2 project.
66644 additional projects are related by organism.
Phenotypic and genotypic description of AUTS2 deletion patients found by Array analysis in an international cohort of intellectual disability (ID) and multiple congenital malformations (MCA). More...
AccessionPRJNA170386; GEO: GSE37142
Data TypeVariation
ScopeMonoisolate
OrganismHomo sapiens[Taxonomy ID: 9606]
Eukaryota; Metazoa; Chordata; Craniata; Vertebrata; Euteleostomi; Mammalia; Eutheria; Euarchontoglires; Primates; Haplorrhini; Catarrhini; Hominidae; Homo; Homo sapiens
PublicationsBeunders G et al., "Exonic deletions in AUTS2 cause a syndromic form of intellectual disability and suggest a critical role for the C terminus.", Am J Hum Genet, 2013 Feb 7;92(2):210-20
SubmissionRegistration date: 12-Jul-2012
Cytogenetics, Clinical Genetics, VU medical center
RelevanceMedical
Project Data:
Resource NameNumber
of Links
Publications
PubMed1
PMC1
Other datasets
GEO DataSets1
GEO Data Details
ParameterValue
Data volume, Spots2450000
Data volume, Processed Mbytes82
Data volume, Supplementary Mbytes65

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