##fileformat=VCFv4.4
##reference=GRCh38
##ALT=<ID=DUP,Description="Duplication">
##ALT=<ID=DEL,Description="Deletion">
##INFO=<ID=END,Number=1,Type=Integer,Description="End position of the longest variant described in this record">
##INFO=<ID=SVLEN,Number=A,Type=Integer,Description="Length of structural variant">
##INFO=<ID=CN,Number=A,Type=Float,Description="Copy number of CNV/breakpoint">
##INFO=<ID=SVCLAIM,Number=A,Type=String,Description="Claim made by the structural variant call. Valid values are D, J, DJ for abundance, adjacency and both respectively">
##INFO=<ID=IMPRECISE,Number=0,Type=Flag,Description="Imprecise structural variation">
##FORMAT=<ID=GT,Number=1,Type=String,Description="Genotype">
#CHROM	POS	ID	REF	ALT	QUAL	FILTER	FORMAT	INFO	pgxbs-kftviwud
4	925495	.		<DEL>	.	PASS	GT	IMPRECISE;SVCLAIM=D;END=None;SVLEN=1804166	0/1
11	67515830	.		<DUP>	.	PASS	GT	IMPRECISE;SVCLAIM=D;END=None;SVLEN=4990233	0/1
11	130895115	.		<DEL>	.	PASS	GT	IMPRECISE;SVCLAIM=D;END=None;SVLEN=16451	0/1
20	323471	.		<DUP>	.	PASS	GT	IMPRECISE;SVCLAIM=D;END=None;SVLEN=115756	0/1