Variant Details

Variant: esv2291987

Internal ID

7963098

Landmark

Location Information

Type	Coordinates	Assembly	Other Links
Inner	chr1:61617194..61618033	hg38	UCSC Ensembl
Outer	chr1:61617016..61618216	hg38	UCSC Ensembl
Inner	chr1:62082866..62083705	hg19	UCSC Ensembl
Outer	chr1:62082688..62083888	hg19	UCSC Ensembl
Inner	chr1:61855454..61856293	hg18	UCSC Ensembl
Outer	chr1:61855276..61856476	hg18	UCSC Ensembl

Cytoband

1p31.3

Allele length

Assembly	Allele length
hg38	1201
hg19	1201
hg18	1201

Variant Type

CNV deletion

Copy Number

Allele State

Allele Origin

Probe Count

Validation Flag

Merged Status

Merged Variants

Supporting Variants

essv4876772

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)

esv2291987

Frequency

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