Variant Details

Variant: esv2215260

Internal ID

7886371

Landmark

Location Information

Type	Coordinates	Assembly	Other Links
Inner	chr10:116505708..116506121	hg38	UCSC Ensembl
Outer	chr10:116505614..116506188	hg38	UCSC Ensembl
Inner	chr10:118265220..118265633	hg19	UCSC Ensembl
Outer	chr10:118265126..118265700	hg19	UCSC Ensembl
Inner	chr10:118255210..118255623	hg18	UCSC Ensembl
Outer	chr10:118255116..118255690	hg18	UCSC Ensembl

Cytoband

10q25.3

Allele length

Assembly	Allele length
hg38	575
hg19	575
hg18	575

Variant Type

CNV deletion

Copy Number

Allele State

Allele Origin

Probe Count

Validation Flag

Merged Status

Merged Variants

Supporting Variants

essv4654803

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)

esv2215260

Frequency

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