Variant DetailsVariant: esv2731810| Internal ID | 9966128 | | Landmark | | | Location Information | | | Cytoband | 6p21.33 | | Allele length | | Assembly | Allele length | | hg38 | 178 | | hg19 | 178 |
| | Variant Type | CNV deletion | | Copy Number | | | Allele State | | | Allele Origin | | | Probe Count | | | Validation Flag | | | Merged Status | M | | Merged Variants | | | Supporting Variants | essv6872674, essv6676491, essv6893492, essv6808356, essv6899645, essv6826333, essv6786334, essv6694110, essv6671048, essv6715470, essv6690373 | | Samples | SSM100, SSM036, SSM075, SSM069, SSM032, SSM031, SSM080, SSM037, SSM091, SSM043, SSM098 | | Known Genes | | | Method | Sequencing | | Analysis | Breakdancer:4 times standard deviation,VariationHunter:4 times standard deviation and at least 3 supportting reads | | Platform | Illumina HiSeq 2000 | | Comments | | | Reference | Wong_et_al_2012b | | Pubmed ID | 23290073 | | Accession Number(s) | esv2731810
| | Frequency | | Sample Size | 96 | | Observed Gain | 0 | | Observed Loss | 11 | | Observed Complex | 0 | | Frequency | n/a |
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