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List of identified structural variations (SVs) and single nucleotide variations (SNVs).
Click the links for details and/or information.
chr	SV	SNV
chr1	completed	432
chr2	completed	138
chr3	completed	249
chr4	completed	244
chr5	completed	321
chr6	partially completed	253
chr7	partially completed	241
chr8	partially completed	261
chr9	partially completed	295
chr10	in progress	351
chr11	in progress	116
chr12	in progress	168
chr13	in progress	154
chr14	in progress	176
chr15	in progress	153
chr16	in progress	270
chr17	completed	297
chr18	completed	149
chr19	completed	94
chrX	completed	233
chrY*	n.d.	6*
		SNV spectrum
SVs and SNV were identified by IGV browzer and samtools, respectively. Approximately 2/3 of SV detection were completed. All the SNV detection were accomplished. No experimental valications have been conducted, yet. The numbers in the SNV column indicate the SNV calls on each chromosome.
*A female genomic DNA sample was used for WGS; therefore, the six SNVs found on chrY were eliminated for further analysis.