A curated catalogue of human genomic structural variation




Variant Details

Variant: esv22237



Internal ID11386156
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:31372231..31375929hg38UCSC Ensembl
Innerchr11:31393778..31397476hg19UCSC Ensembl
Innerchr11:31350354..31354052hg18UCSC Ensembl
Cytoband11p13
Allele length
AssemblyAllele length
hg383699
hg193699
hg183699
Variant TypeCNV gain+loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsesv14498
SamplesNA18502, NA11995, NA18861, NA18508, NA19190, NA18916, NA12287, NA12828, NA12489, NA18907, NA19114, NA15510, NA19099, NA19257, NA19225, NA18858, NA18909, NA19108, NA19240, NA07037, NA12749, NA18505, NA19129, NA12006, NA18511, NA12776
Known GenesDNAJC24
MethodOligo aCGH
AnalysisSegment log2 ratios from each sample. This was done running the GADA algorithm (Pique-Regi et al., 2008) using the options "-M 10 -T 10 -a 2.5". Filter non-CNV segments using intensity thresholds. Merge remaining CNV "calls" within each sample. Adjacent calls of the same direction (gain or loss) are merged if both: the distance between calls is less than 10kb, and the distance between calls is less than 10% of the size of the largest of the two calls.
PlatformSanger H. Sapiens 42mCGH Array 5781_53 726K v1
Comments
ReferenceConrad_et_al_2009
Pubmed ID19812545
Accession Number(s)esv22237
Frequency
Sample Size40
Observed Gain25
Observed Loss1
Observed Complex0
Frequencyn/a


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