Variant DetailsVariant: esv2743970| Internal ID | 9978254 | | Landmark | | | Location Information | | | Cytoband | 11p15.5 | | Allele length | | Assembly | Allele length | | hg38 | 612 | | hg19 | 612 |
| | Variant Type | CNV deletion | | Copy Number | | | Allele State | | | Allele Origin | | | Probe Count | | | Validation Flag | | | Merged Status | M | | Merged Variants | | | Supporting Variants | essv6740895, essv6749536, essv6863997, essv6775546, essv6771889, essv6856906, essv6958966, essv6746682, essv6827505 | | Samples | SSM011, SSM065, SSM087, SSM026, SSM066, SSM080, SSM055, SSM052, SSM056 | | Known Genes | LSP1 | | 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) | esv2743970
| | Frequency | | Sample Size | 96 | | Observed Gain | 0 | | Observed Loss | 9 | | Observed Complex | 0 | | Frequency | n/a |
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