MOESM4 of Inter- and intra-breed genome-wide copy number diversity in a large cohort of European equine breeds

Additional file 4: Table S3. Genomic regions validated for CNVs by RT-qPCR. Primer sequences, position, product size, annealing temperature and TaqMan probes are shown. The CNV status in the SNP-array and in the qPCR and the CNV validation by qPCR are given. Table S4. Results of quantitative PCR. The results of the four CNVs per each horse and the outcome of the validation through qPCR are presented.

附加文件4：表S3。经逆转录实时定量聚合酶链反应（RT-qPCR）验证的拷贝数变异（Copy Number Variation，CNV）基因组区域。本表格包含引物序列、引物位置、扩增产物长度、退火温度及TaqMan探针的相关信息，同时给出了单核苷酸多态性芯片（SNP-array）与定量聚合酶链反应（qPCR）检测所得的CNV状态，以及通过qPCR完成的CNV验证结果。

表S4。定量PCR检测结果。本表格呈现了每匹马的4种CNV检测结果，以及通过qPCR完成的验证结果。