Variant Details

Variant: esv2761167

Internal ID

10377474

Landmark

Location Information

Type	Coordinates	Assembly	Other Links
Inner	chr8:106833977..106851468	hg38	UCSC Ensembl
Inner	chr8:107846205..107863696	hg19	UCSC Ensembl
Inner	chr8:107915381..107932872	hg18	UCSC Ensembl

Cytoband

8q23.1

Allele length

Assembly	Allele length
hg38	17492
hg19	17492
hg18	17492

Variant Type

CNV loss

Copy Number

Allele State

Allele Origin

Probe Count

Validation Flag

Merged Status

Merged Variants

Supporting Variants

essv7017148, essv7017147, essv7017136, essv7017141, essv7017161, essv7017127, essv7017143, essv7017150, essv7017142, essv7017162, essv7017156, essv7017157, essv7017130, essv7017139, essv7017158, essv7017137, essv7017140, essv7017138, essv7017135, essv7017129, essv7017151, essv7017149, essv7017132, essv7017153, essv7017134, essv7017128, essv7017159, essv7017163, essv7017145, essv7017146, essv7017154, essv7017131, essv7017152, essv7017160

Samples

RW_0123, RW_0300, RW_0087, RW_0644, RW_0058, RW_0007, RW_0268, RW_0604, RW_0322, RW_0330, RW_0658, RW_0357, RW_0111, RW_0500, RW_0155, RW_0299, RW_0302, RW_0177, RW_0310, RW_0664, RW_0653, RW_0092, RW_0053, RW_0195, RW_0120, RW_0200, RW_0220, RW_0238, RW_0183, RW_0154, RW_0234, RW_0018, RW_0508, RW_0550

Known Genes

Method

Merging

Analysis

Two different algorithms (PennCNV and Birdseye) were applied to detect CNVs. Only congruent CNV events regarding direction of effect that were detected by both algorithms were merged using the outer borders of the event in a first step. In a second step only CNVs that were detected in at least two individuals were merged into a CNVR.

Platform

Merging

Comments

Reference

Vogler_et_al_2010

Pubmed ID

21179565

Accession Number(s)

esv2761167

Frequency

Sample Size	1109
Observed Gain	0
Observed Loss	34
Observed Complex	0
Frequency	n/a