A curated catalogue of human genomic structural variation




Variant Details

Variant: essv61620



Internal ID10988171
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr12:120902721..120904404hg38UCSC Ensembl
Innerchr12:121340524..121342207hg19UCSC Ensembl
Innerchr12:119824907..119826590hg18UCSC Ensembl
Cytoband12q24.31
Allele length
AssemblyAllele length
hg381684
hg191684
hg181684
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv19320
Supporting Variants
SamplesNA12239
Known GenesSPPL3
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)essv61620
Frequency
Sample Size40
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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