A curated catalogue of human genomic structural variation




Variant Details

Variant: esv11794



Internal ID11375713
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr1:149033410..149035524hg19UCSC Ensembl
Innerchr1:147300034..147302148hg18UCSC Ensembl
Cytoband1q21.1
Allele length
AssemblyAllele length
hg192115
hg182115
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsesv21838
Supporting Variantsessv70293, essv36488
SamplesNA18916, NA18907
Known GenesLOC101929780
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)esv11794
Frequency
Sample Size40
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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