Variant Details

Variant: esv1935496

Internal ID

7259921

Landmark

Location Information

Type	Coordinates	Assembly	Other Links
Inner	chr18:13887045..13887257	hg38	UCSC Ensembl
Outer	chr18:13886958..13887311	hg38	UCSC Ensembl
Inner	chr18:13887044..13887256	hg19	UCSC Ensembl
Outer	chr18:13886957..13887310	hg19	UCSC Ensembl
Inner	chr18:13877044..13877256	hg18	UCSC Ensembl
Outer	chr18:13876957..13877310	hg18	UCSC Ensembl

Cytoband

18p11.21

Allele length

Assembly	Allele length
hg38	354
hg19	354
hg18	354

Variant Type

CNV deletion

Copy Number

Allele State

Allele Origin

Probe Count

Validation Flag

Merged Status

Merged Variants

Supporting Variants

essv4603786

Samples

NA18507

Known Genes

MC2R

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)

esv1935496

Frequency

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