Variant DetailsVariant: esv2758021![](http://dgv.tcag.ca/gb2/gbrowse_img/dgv2_hg18/?name=chr5:149804786..150265935;width=800;overview=1) Internal ID | 9633480 | Landmark | | Location Information | | Cytoband | 5q33.1 | Allele length | Assembly | Allele length | hg38 | 461151 | hg19 | 461150 | hg18 | 461150 | hg17 | 461150 |
| Variant Type | CNV loss | Copy Number | | Allele State | | Allele Origin | | Probe Count | | Validation Flag | | Merged Status | M | Merged Variants | esv2759386 | Supporting Variants | essv12514, essv1590, essv11956, essv4031, essv6300, essv5740, essv10896, essv15413, essv4648, essv1506, essv16466, essv5188, essv4415, essv11552, essv8204, essv14321, essv9040, essv16516, essv13730, essv2891, essv5443, essv16853, essv7171, essv10215, essv16732, essv15549, essv18770, essv12823, essv10379, essv9612, essv8434, essv5359, essv14624, essv6758, essv580, essv2330, essv17040, essv1826, essv13831, essv7575, essv15074, essv7358, essv3390, essv21999, essv15345, essv9979, essv1237, essv8943, essv2639, essv11436, essv14722, essv5046, essv17323, essv12655, essv14873, essv4001, essv2040, essv15218, essv14431, essv13439, essv12542, essv17012, essv16337, essv859, essv306, essv3703, essv10628, essv5237, essv2776, essv8362, essv9799, essv3887, essv15687, essv16068, essv9406, essv6399, essv13130, essv11149, essv8107, essv7008, essv1017, essv2591, essv15458, essv10543, essv4172, essv13566, essv12392, essv8743, essv10434, essv10117, essv6900, essv2445, essv20353, essv3824, essv14537, essv14104, essv16204, essv14137, essv4708, essv9386, essv1790, essv10726, essv16097, essv6036, essv15730, essv1135, essv7137, essv13639, essv10841, essv1956, essv4959, essv17148 | Samples | NA18998, NA18502, NA19141, NA19222, NA19203, NA18947, NA11995, NA18862, NA18861, NA18980, NA18855, NA12236, NA18999, NA19092, NA18545, NA18959, NA19098, NA18967, NA18563, NA19127, NA19192, NA19171, NA19005, NA18940, NA19201, NA18995, NA19119, NA18635, NA18547, NA19131, NA18942, NA18571, NA18964, NA19130, NA18949, NA18611, NA18970, NA19137, NA19238, NA19207, NA19172, NA19159, NA18990, NA19209, NA19200, NA18605, NA19210, NA19120, NA19194, NA19152, NA19161, NA18515, NA19205, NA18516, NA18637, NA18871, NA18572, NA18976, NA19208, NA19202, NA18537, NA18573, NA19142, NA19000, NA18856, NA18912, NA18857, NA18853, NA19099, NA18555, NA18523, NA19160, NA19132, NA18570, NA18858, NA18593, NA18945, NA18576, NA18953, NA19094, NA18978, NA18632, NA19206, NA18863, NA19140, NA19240, NA19100, NA19144, NA18943, NA19193, NA12874, NA18594, NA18501, NA19173, NA18987, NA19211, NA18994, NA19093, NA18500, NA18609, NA19102, NA18854, NA19116, NA18505, NA19129, NA18624, NA19139, NA18522, NA18612, NA18622, NA18562, NA18997 | Known Genes | DCTN4, IRGM, LOC102546298, MYOZ3, NDST1, RBM22, RPS14, SMIM3, SYNPO, ZNF300 | Method | BAC aCGH | Analysis | Array images were acquired using an Agilent laser scanner (Agilent Technologies, UK). Fluorescence intensities and log2 ratio values were extracted using Bluefuse software (Bluegnome Ltd). | Platform | Agilent | Comments | | Reference | Redon_et_al_2006 | Pubmed ID | 17122850 | Accession Number(s) | esv2758021
| Frequency | Sample Size | 270 | Observed Gain | 0 | Observed Loss | 112 | Observed Complex | 0 | Frequency | n/a |
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