A curated catalogue of human genomic structural variation




Variant Details

Variant: esv26690



Internal ID11043923
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:86055238..86058859hg38UCSC Ensembl
Innerchr4:86976391..86980012hg19UCSC Ensembl
Innerchr4:87195415..87199036hg18UCSC Ensembl
Cytoband4q21.3
Allele length
AssemblyAllele length
hg383622
hg193622
hg183622
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsesv15242
SamplesNA18523, NA12776, NA19108, NA18508, NA18916, NA19190, NA18858, NA18907, NA12878, NA19240
Known GenesMAPK10
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)esv26690
Frequency
Sample Size40
Observed Gain0
Observed Loss10
Observed Complex0
Frequencyn/a


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