My suspicion was correct, but there is a more straightforward way to confirm it.
From the header of the VCF file produced by Dindel:
Code:
##INFO=<ID=[B]DP[/B],Number=1,Type=Integer,Description="[B]Total number of reads in haplotype window[/B]">
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##INFO=<ID=[B]DP[/B],Number=1,Type=Integer,Description="[B]Total number of reads in haplotype window[/B]">
#CHROM POS ID REF ALT QUAL FILTER INFO FORMAT SAMPLE chromosome_II 6680 . TATA T 118 PASS DP=230;NF=0;NR=3;NRS=13;NFS=23;HP=1 GT:GQ 0/1:118
(...) **** tid: chromosome_II [B]pos: 6681 leftPos: 6620 rightPos: 6742[/B] Fetching reads.... [B]Number of reads: 230[/B] out of 77463 # unmapped reads: 0 numReadsUnknownLib: 0 numChrMismatch: 0 numMappedWithoutMate: 2 numUnmappedWithoutMate: 0 candidate_var@pos: 6681 6680,-ATA aligned_var@pos 6681 6656 A=>G aligned_var@pos 6681 6657 T=>A aligned_var@pos 6681 6680 -ATA [empiricalDistributionMethod] Number of haplotypes: 8 Filtered 0 haplotypes. ll_ref: -1085.49 max_ll_indel: -1058.3 qual: 118.099 (...)
chr19 11243209 . c cG 128 PASS DP=12;NF=0;NR=4;NRS=3;NFS=1;HP=1 GT:GQ 1/1:12
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