Variant Details

Variant: esv25027

Internal ID

11388946

Landmark

Location Information

Type	Coordinates	Assembly	Other Links
Inner	chr8:11378889..11389622	hg38	UCSC Ensembl
Inner	chr8:11236398..11247131	hg19	UCSC Ensembl
Inner	chr8:11273808..11284541	hg18	UCSC Ensembl

Cytoband

8p23.1

Allele length

Assembly	Allele length
hg38	10734
hg19	10734
hg18	10734

Variant Type

CNV loss

Copy Number

Allele State

Allele Origin

Probe Count

Validation Flag

Merged Status

Merged Variants

Supporting Variants

esv10439, esv13863

Samples

NA18502, NA11995, NA18861, NA18508, NA12414, NA12004, NA19190, NA18916, NA12156, NA12044, NA11993, NA12489, NA12878, NA18907, NA07045, NA19114, NA11894, NA12239, NA19099, NA19257, NA19225, NA06985, NA18523, NA18858, NA18909, NA19108, NA19147, NA18517, NA19240, NA07037, NA12749, NA18505, NA19129, NA12006, NA12776

Known Genes

C8orf12

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)

esv25027

Frequency

Sample Size	40
Observed Gain	0
Observed Loss	35
Observed Complex	0
Frequency	n/a