A curated catalogue of human genomic structural variation




Variant Details

Variant: esv10580



Internal ID11027814
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr1:586033..639715hg38UCSC Ensembl
Innerchr1:521413..575095hg19UCSC Ensembl
Innerchr1:511276..564958hg18UCSC Ensembl
Cytoband1p36.33
Allele length
AssemblyAllele length
hg3853683
hg1953683
hg1853683
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsesv21732
Supporting Variantsessv39460, essv57440, essv51804, essv68086, essv36813, essv75601, essv61475, essv56439, essv81202, essv79491, essv58239
SamplesNA12414, NA12287, NA11993, NA19114, NA11894, NA12239, NA18858, NA19108, NA12749, NA12006, NA12776
Known GenesMIR6723
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)esv10580
Frequency
Sample Size40
Observed Gain0
Observed Loss11
Observed Complex0
Frequencyn/a


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