Variant Details

Variant: essv4607699

Internal ID

7193331

Landmark

Location Information

Type	Coordinates	Assembly	Other Links
Inner	chr6:138626609..138626929	hg38	UCSC Ensembl
Outer	chr6:138626421..138627117	hg38	UCSC Ensembl
Inner	chr6:138947746..138948066	hg19	UCSC Ensembl
Outer	chr6:138947558..138948254	hg19	UCSC Ensembl
Inner	chr6:138989439..138989759	hg18	UCSC Ensembl
Outer	chr6:138989251..138989947	hg18	UCSC Ensembl

Cytoband

6q23.3

Allele length

Assembly	Allele length
hg38	697
hg19	697
hg18	697

Variant Type

CNV deletion

Copy Number

Allele State

Allele Origin

Probe Count

Validation Flag

Merged Status

Merged Variants

esv2096132

Supporting Variants

Samples

NA18507

Known Genes

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)

essv4607699

Frequency

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