Variant Details

Variant: esv19157

Internal ID

11036391

Landmark

Location Information

Type	Coordinates	Assembly	Other Links
Inner	chr13:114198348..114200349	hg38	UCSC Ensembl
Inner	chr13:114963823..114965824	hg19	UCSC Ensembl
Inner	chr13:113981925..113983926	hg18	UCSC Ensembl

Cytoband

13q34

Allele length

Assembly	Allele length
hg38	2002
hg19	2002
hg18	2002

Variant Type

CNV loss

Copy Number

Allele State

Allele Origin

Probe Count

Validation Flag

Merged Status

Merged Variants

esv25715

Supporting Variants

essv47273, essv78564, essv82952, essv73889, essv45388, essv69952, essv79188, essv81497, essv67413, essv56928, essv44084

Samples

NA18861, NA19190, NA12156, NA12044, NA12828, NA11993, NA12489, NA19114, NA06985, NA12749, NA19129

Known Genes

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)

esv19157

Frequency

Sample Size	40
Observed Gain	0
Observed Loss	11
Observed Complex	0
Frequency	n/a