A curated catalogue of human genomic structural variation




Variant Details

Variant: esv11323



Internal ID11028557
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr1:12823464..12954384hg38UCSC Ensembl
Innerchr1:12883327..13021370hg19UCSC Ensembl
Innerchr1:12805914..12943957hg18UCSC Ensembl
Cytoband1p36.21
Allele length
AssemblyAllele length
hg38130921
hg19138044
hg18138044
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsesv28644
Supporting Variantsessv33676, essv63729, essv68206, essv71405, essv56267, essv59569, essv59512, essv76814, essv34550, essv79200, essv40866, essv35999, essv38177, essv50799, essv52402, essv48329, essv43168, essv72864
SamplesNA18502, NA11931, NA18916, NA12878, NA18907, NA07045, NA19257, NA19225, NA18523, NA18858, NA18909, NA19108, NA19147, NA07037, NA12749, NA12006, NA18511, NA12776
Known GenesHNRNPCL1, LOC649330, PRAMEF10, PRAMEF11, PRAMEF2, PRAMEF4, PRAMEF6, PRAMEF7, PRAMEF8
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)esv11323
Frequency
Sample Size40
Observed Gain18
Observed Loss0
Observed Complex0
Frequencyn/a


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