Variant Details

Variant: esv2162659

Internal ID

7833770

Landmark

Location Information

Type	Coordinates	Assembly	Other Links
Inner	chr18:54426599..54430588	hg38	UCSC Ensembl
Outer	chr18:54426408..54430784	hg38	UCSC Ensembl
Inner	chr18:51952969..51956958	hg19	UCSC Ensembl
Outer	chr18:51952778..51957154	hg19	UCSC Ensembl
Inner	chr18:50206967..50210956	hg18	UCSC Ensembl
Outer	chr18:50206776..50211152	hg18	UCSC Ensembl

Cytoband

18q21.2

Allele length

Assembly	Allele length
hg38	4377
hg19	4377
hg18	4377

Variant Type

CNV deletion

Copy Number

Allele State

Allele Origin

Probe Count

Validation Flag

Merged Status

Merged Variants

Supporting Variants

essv4704309

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)

esv2162659

Frequency

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