Variant Details

Variant: esv2385250

Internal ID

7709675

Landmark

Location Information

Type	Coordinates	Assembly	Other Links
Inner	chr6:131482076..131482302	hg38	UCSC Ensembl
Outer	chr6:131482001..131482363	hg38	UCSC Ensembl
Inner	chr6:131803216..131803442	hg19	UCSC Ensembl
Outer	chr6:131803141..131803503	hg19	UCSC Ensembl
Inner	chr6:131844909..131845135	hg18	UCSC Ensembl
Outer	chr6:131844834..131845196	hg18	UCSC Ensembl

Cytoband

6q23.2

Allele length

Assembly	Allele length
hg38	363
hg19	363
hg18	363

Variant Type

CNV deletion

Copy Number

Allele State

Allele Origin

Probe Count

Validation Flag

Merged Status

Merged Variants

dgv33e194

Supporting Variants

essv4745121

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)

esv2385250

Frequency

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