Variant Details

Variant: esv3303842

Internal ID

15150790

Landmark

Location Information

Type	Coordinates	Assembly	Other Links
	chr11:110507149..110507150	hg38	UCSC Ensembl
Inner	chr11:110507132..110507167	hg38	UCSC Ensembl
Outer	chr11:110507131..110507168	hg38	UCSC Ensembl
	chr11:110377873..110377874	hg19	UCSC Ensembl
Inner	chr11:110377856..110377891	hg19	UCSC Ensembl
Outer	chr11:110377855..110377892	hg19	UCSC Ensembl
	chr11:109883083..109883084	hg18	UCSC Ensembl
Inner	chr11:109883101..109883066	hg18	UCSC Ensembl
Outer	chr11:109883065..109883102	hg18	UCSC Ensembl

Cytoband

11q22.3

Allele length

Assembly	Allele length
hg38	6056
hg19	6056
hg18	6056

Variant Type

CNV mobile element insertion

Copy Number

Allele State

Allele Origin

Probe Count

Validation Flag

Merged Status

Merged Variants

Supporting Variants

essv7814978, essv7772393, essv7811085, essv7783299, essv7825362, essv7809468, essv7788378, essv7830937, essv7814244, essv7807721, essv7796608, essv7835496, essv7827862, essv7826580, essv7786931, essv7834557, essv7805632, essv7771595, essv7811741, essv7780360, essv7830030, essv7816465, essv7792044, essv7830545, essv7820644, essv7818400, essv7800548, essv7794023, essv7799168, essv7803542, essv7773539, essv7792873, essv7789394, essv7775073, essv7824126, essv7777770, essv7807210, essv7795559, essv7797031, essv7778993, essv7828829, essv7815725, essv7800283, essv7822678, essv7831824, essv7781565, essv7788888, essv7777624, essv7796371, essv7784448, essv7786677, essv7774707, essv7819325, essv7818709, essv7804079, essv7790339, essv7774413, essv7780115

Samples

NA18502, NA18561, NA18507, NA11920, NA12751, NA12004, NA18959, NA19190, NA18870, NA07346, NA18563, NA18550, NA18519, NA12891, NA18960, NA18942, NA11918, NA19138, NA18498, NA18964, NA12761, NA18970, NA19137, NA11994, NA18973, NA11993, NA11831, NA10847, NA18951, NA12003, NA12878, NA18956, NA18516, NA18579, NA18948, NA18537, NA19114, NA11919, NA12892, NA18532, NA19257, NA19225, NA12144, NA18593, NA18608, NA18542, NA11881, NA18961, NA18952, NA19147, NA18564, NA06986, NA19093, NA18505, NA19129, NA12776, NA18965, NA18577

Known Genes

Method

Sequencing

Analysis

Platform

Roche 454

Comments

Reference

1000_Genomes_Consortium_Pilot_Project

Pubmed ID

20981092

Accession Number(s)

esv3303842

Frequency

Sample Size	185
Observed Gain	58
Observed Loss	0
Observed Complex	0
Frequency	n/a