A curated catalogue of human genomic structural variation




Variant Details

Variant: esv13521



Internal ID11377440
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:54525183..54538133hg38UCSC Ensembl
Innerchr11:51581147..51594097hg19UCSC Ensembl
Innerchr11:51437723..51450673hg18UCSC Ensembl
Cytoband11p11.11
Allele length
AssemblyAllele length
hg3812951
hg1912951
hg1812951
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsesv29682
Supporting Variantsessv75354, essv76048, essv80958, essv39053, essv40593, essv61947, essv77418, essv37259
SamplesNA11995, NA12414, NA12004, NA12287, NA12878, NA11894, NA12239, NA18511
Known Genes
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)esv13521
Frequency
Sample Size40
Observed Gain8
Observed Loss0
Observed Complex0
Frequencyn/a


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