A curated catalogue of human genomic structural variation




Variant Details

Variant: essv51572



Internal ID11326793
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:66944678..66945736hg38UCSC Ensembl
Innerchr11:66712149..66713207hg19UCSC Ensembl
Innerchr11:66468725..66469783hg18UCSC Ensembl
Cytoband11q13.1
Allele length
AssemblyAllele length
hg381059
hg191059
hg181059
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag1
Merged StatusS
Merged Variantsesv13515
Supporting Variants
SamplesNA11931
Known GenesPC
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)essv51572
Frequency
Sample Size40
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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