A curated catalogue of human genomic structural variation




Variant Details

Variant: esv16892



Internal ID11034126
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr1:91766526..91767865hg38UCSC Ensembl
Innerchr1:92232083..92233422hg19UCSC Ensembl
Innerchr1:92004671..92006010hg18UCSC Ensembl
Cytoband1p22.1
Allele length
AssemblyAllele length
hg381340
hg191340
hg181340
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsesv25877
Supporting Variantsessv36563, essv79989, essv52322, essv39316, essv73486, essv59425, essv40704, essv62852, essv64629, essv51120, essv55586, essv78286, essv75340, essv75829, essv77335, essv66658, essv44576, essv38106, essv41141, essv69796, essv57958, essv43495
SamplesNA11995, NA12414, NA11931, NA12004, NA12287, NA12156, NA12044, NA12828, NA11993, NA12489, NA12878, NA07045, NA11894, NA15510, NA19099, NA19257, NA06985, NA18909, NA19108, NA18505, NA12006, NA18511
Known GenesTGFBR3
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)esv16892
Frequency
Sample Size40
Observed Gain0
Observed Loss22
Observed Complex0
Frequencyn/a


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