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. 2015 Apr 22;7(4):3054–3066. doi: 10.3390/nu7043054

Table 1.

Basic information of selected candidate CNV loci.

CNV_ID Locus Position * Size (bp) Overlap Genes
CNV_1 11q11 chr11: 55,130,596–55,210,165 79,569 OR4P1P OR4V1P OR4P4 OR4S2 OR4C6
CNV_2 5q13.2 chr5: 68,903,038–70,343,313 1,440,275 SMN1 SMN2 SERF1A SMA4 SMA5 GUSBP1 LOC643367 LOC643784 LOC653080 LOC653188 GTF2H2B LOC653391 LOC728488 SERF1B LOC728499 LOC728506 LOC728519 LOC728526 LOC728535 LOC728555 LOC100093625 LOC100132218 LOC100133280
CNV_4 10q11.22(1) chr10: 46,338,178–46,812,351 474,173 GLUDP2 PPYR1 GPRIN2 SYT15 BMS1P2 LOC642826 LOC643650 ANXA8L1 CTGLF7 LOC728643 LOC728657 LOC100132646 FAM25B LOC100133189
CNV_10 10q11.22(2) chr10: 47,011,183–47,145,122 133,939 LOC340844 LOC728684
CNV_12 6q14.1 chr6: 81,340,896–81,346,266 5370 None
CNV_13 4q25 chr4: 108,285,188–108,293,270 8082 None

* Chromosome positions were based on 2006 (NCBI36/hg18); CNV, copy number variation.