Homo sapiens (ID 170382) - BioProject

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Accession: PRJNA170382 ID: 170382

Homo sapiens (human)

Oligo array for CNV calling AUTS2 project [Agilent]

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.

95506 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...

Accession	PRJNA170382; GEO: GSE37141
Data Type	Variation
Scope	Multiisolate
Organism	Homo sapiens[Taxonomy ID: 9606] Eukaryota; Metazoa; Chordata; Craniata; Vertebrata; Euteleostomi; Mammalia; Eutheria; Euarchontoglires; Primates; Haplorrhini; Catarrhini; Hominidae; Homo; Homo sapiens
Publications	Beunders 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
Submission	Registration date: 12-Jul-2012 Cytogenetics, Clinical Genetics, VU medical center
Relevance	Medical

Project Data:

Resource Name	Number of Links
Publications
PubMed	1
PMC	1
Other datasets
GEO DataSets	1

GEO Data Details

Parameter	Value
Data volume, Spots	203648
Data volume, Processed Mbytes	4
Data volume, Supplementary Mbytes	43

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Homo sapiens (human)

Oligo array for CNV calling AUTS2 project [Agilent]

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