Variant Details

Variant: essv4668978

Internal ID

7254610

Landmark

Location Information

Type	Coordinates	Assembly	Other Links
Inner	chr11:75541961..75542109	hg38	UCSC Ensembl
Outer	chr11:75541838..75542283	hg38	UCSC Ensembl
Inner	chr11:75253006..75253154	hg19	UCSC Ensembl
Outer	chr11:75252883..75253328	hg19	UCSC Ensembl
Inner	chr11:74930654..74930802	hg18	UCSC Ensembl
Outer	chr11:74930531..74930976	hg18	UCSC Ensembl

Cytoband

11q13.5

Allele length

Assembly	Allele length
hg38	446
hg19	446
hg18	446

Variant Type

CNV deletion

Copy Number

Allele State

Allele Origin

Probe Count

Validation Flag

Merged Status

Merged Variants

esv1986553

Supporting Variants

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)

essv4668978

Frequency

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