Variant Details

Variant: esv2109973

Internal ID

7434398

Landmark

Location Information

Type	Coordinates	Assembly	Other Links
Inner	chr6:41643518..41643593	hg38	UCSC Ensembl
Outer	chr6:41643341..41643778	hg38	UCSC Ensembl
Inner	chr6:41611256..41611331	hg19	UCSC Ensembl
Outer	chr6:41611079..41611516	hg19	UCSC Ensembl
Inner	chr6:41719234..41719309	hg18	UCSC Ensembl
Outer	chr6:41719057..41719494	hg18	UCSC Ensembl

Cytoband

6p21.1

Allele length

Assembly	Allele length
hg38	438
hg19	438
hg18	438

Variant Type

CNV deletion

Copy Number

Allele State

Allele Origin

Probe Count

Validation Flag

Merged Status

Merged Variants

Supporting Variants

essv4998301

Samples

NA18507

Known Genes

MDFI

Method

Sequencing

Analysis

Hierarchical clustering of anomalous readpairs was used to identify groupings of five or more readpairs that had a similar size and position. Read pairs were defined as anomalous if they had high-confidence alignments of each individual read that nevertheless were either incorrectly oriented or implied an insert size of at least 3 standard deviations outside the sample median.

Platform

Not specified

Comments

Reference

Bentley_et_al_2008

Pubmed ID

18987734

Accession Number(s)

esv2109973

Frequency

Sample Size	1
Observed Gain	0
Observed Loss	1
Observed Complex	0
Frequency	n/a