A curated catalogue of human genomic structural variation




Variant Details

Variant: essv59899



Internal ID11005924
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
InnerchrX:134854869..134971089hg19UCSC Ensembl
InnerchrX:134682535..134798755hg18UCSC Ensembl
CytobandXq26.3
Allele length
AssemblyAllele length
hg19116221
hg18116221
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag1
Merged StatusS
Merged Variantsesv13047
Supporting Variants
SamplesNA18523
Known GenesCT45A1, CT45A2, CT45A3, CT45A4, CT45A5, CT45A6
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)essv59899
Frequency
Sample Size40
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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