Variant Details

Variant: esv17449

Internal ID

11381368

Landmark

Location Information

Type	Coordinates	Assembly	Other Links
Inner	chr18:76392941..76394806	hg38	UCSC Ensembl
Inner	chr18:74104897..74106762	hg19	UCSC Ensembl
Inner	chr18:72233885..72235750	hg18	UCSC Ensembl

Cytoband

18q23

Allele length

Assembly	Allele length
hg38	1866
hg19	1866
hg18	1866

Variant Type

CNV gain

Copy Number

Allele State

Allele Origin

Probe Count

Validation Flag

Merged Status

Merged Variants

esv28838

Supporting Variants

essv78562, essv67516, essv38274, essv43987, essv75469, essv40634, essv56391, essv61893, essv72859, essv83948, essv65202, essv33269, essv49721, essv79190, essv42357, essv66966, essv70161, essv51597, essv73764, essv54762, essv62247, essv60091, essv47224, essv70002, essv81482, essv80661, essv53453

Samples

NA11995, NA18861, NA18508, NA12414, NA11931, NA19190, NA18916, NA12156, NA12044, NA12828, NA12878, NA19114, NA12239, NA15510, NA19099, NA19257, NA19225, NA06985, NA18523, NA18858, NA18909, NA19147, NA18517, NA19240, NA12749, NA18505, NA12776

Known Genes

ZNF516

Method

Oligo aCGH

Analysis

Segment 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.

Platform

Sanger H. Sapiens 42mCGH Array 5781_53 726K v1

Comments

Reference

Conrad_et_al_2009

Pubmed ID

19812545

Accession Number(s)

esv17449

Frequency

Sample Size	40
Observed Gain	27
Observed Loss	0
Observed Complex	0
Frequency	n/a