A curated catalogue of human genomic structural variation




Variant Details

Variant: esv17859



Internal ID11035093
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr18:4330259..4335790hg38UCSC Ensembl
Innerchr18:4330259..4335790hg19UCSC Ensembl
Innerchr18:4320259..4325790hg18UCSC Ensembl
Cytoband18p11.31
Allele length
AssemblyAllele length
hg385532
hg195532
hg185532
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsesv28168
Supporting Variantsessv38626, essv68037
SamplesNA19257, NA18858
Known GenesDLGAP1
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)esv17859
Frequency
Sample Size40
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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