Variant DetailsVariant: esv2716258 Internal ID | 9950546 | Landmark | | Location Information | | Cytoband | 17q25.1 | Allele length | Assembly | Allele length | hg38 | 729 | hg19 | 729 |
| Variant Type | CNV deletion | Copy Number | | Allele State | | Allele Origin | | Probe Count | | Validation Flag | | Merged Status | M | Merged Variants | | Supporting Variants | essv6954025, essv6960498, essv6925042, essv6717544, essv6882841, essv6901972, essv6776395, essv6732878, essv6809926, essv6744502, essv6750155, essv6725215, essv6753070, essv6852337, essv6688865, essv6971601, essv6928544, essv6780181, essv6778443, essv6832008, essv6665894 | Samples | SSM008, SSM075, SSM045, SSM057, SSM028, SSM047, SSM018, SSM029, SSM026, SSM019, SSM035, SSM094, SSM067, SSM086, SSM066, SSM081, SSM053, SSM025, SSM043, SSM056, SSM012 | Known Genes | MXRA7 | 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) | esv2716258
| Frequency | Sample Size | 96 | Observed Gain | 0 | Observed Loss | 21 | Observed Complex | 0 | Frequency | n/a |
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