A curated catalogue of human genomic structural variation




Variant Details

Variant: esv24599



Internal ID11388518
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr22:37097648..37098328hg38UCSC Ensembl
Innerchr22:37493688..37494368hg19UCSC Ensembl
Innerchr22:35823634..35824314hg18UCSC Ensembl
Cytoband22q12.3
Allele length
AssemblyAllele length
hg38681
hg19681
hg18681
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsesv12475
SamplesNA12044, NA06985
Known GenesTMPRSS6
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)esv24599
Frequency
Sample Size40
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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