Variant Details

Variant: essv4577815

Internal ID

6816761

Landmark

Location Information

Type	Coordinates	Assembly	Other Links
Inner	chr10:88767660..88767675	hg38	UCSC Ensembl
Outer	chr10:88767451..88767890	hg38	UCSC Ensembl
Inner	chr10:90527417..90527432	hg19	UCSC Ensembl
Outer	chr10:90527208..90527647	hg19	UCSC Ensembl
Inner	chr10:90517397..90517412	hg18	UCSC Ensembl
Outer	chr10:90517188..90517627	hg18	UCSC Ensembl

Cytoband

10q23.31

Allele length

Assembly	Allele length
hg38	440
hg19	440
hg18	440

Variant Type

CNV deletion

Copy Number

Allele State

Allele Origin

Probe Count

Validation Flag

Merged Status

Merged Variants

esv2179332

Supporting Variants

Samples

NA18507

Known Genes

LIPN

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)

essv4577815

Frequency

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