7ae9d0e1bf12e39fc643f806d3251b6e3dca809a
chmalee
  Thu May 21 16:54:10 2020 -0700
Fixing error in size filter for clinGenCnv track, thanks Dan

diff --git src/hg/makeDb/trackDb/human/trackDb.clinGen.ra src/hg/makeDb/trackDb/human/trackDb.clinGen.ra
index 4aa601b..fa8f8a5 100644
--- src/hg/makeDb/trackDb/human/trackDb.clinGen.ra
+++ src/hg/makeDb/trackDb/human/trackDb.clinGen.ra
@@ -1,56 +1,55 @@
 track clinGenSuper
 shortLabel ClinGen
 longLabel Clinical Genome Resource
 group phenDis
 superTrack on
 
     track dosageSensitivity
     parent clinGenSuper on
     shortLabel ClinGen Dosage Sensitivity
     longLabel Clinical Genome Resource Dosage Sensitivity 
     visibility pack
     type bigBed 9 +
     itemRgb on
     compositeTrack on
 
         track clinGenHaplo
         parent dosageSensitivity
         shortLabel ClinGen Haplo Insufficiency
         longLabel ClinGen Haplo Insufficiency
         visibility dense
         type bigBed 9 +
         bigDataUrl /gbdb/$D/bbi/clinGen/clinGenHaplo.bb
         mouseOverField _mouseOver
         filterValues.haploScore 0|No evidence available,1|Little evidence for dosage pathogenicity,2|Some evidence for dosage pathogenicity,3|Sufficient evidence for dosage pathogenicity,30|Gene associated with autosomal recessive phenotype,40|Dosage sensitivity unlikely
         filterLabel.haploScore Haplosensitivity Score
 
         track clinGenTriplo
         parent dosageSensitivity
         shortLabel ClinGen Triplo Sensitivity
         longLabel ClinGen Triplo Sensitivity
         visibility dense
         type bigBed 9 +
         bigDataUrl /gbdb//$D/bbi/clinGen/clinGenTriplo.bb
         mouseOverField _mouseOver
         filterValues.triploScore 0|No evidence available,1|Little evidence for dosage pathogenicity,2|Some evidence for dosage pathogenicity,3|Sufficient evidence for dosage pathogenicity,30|Gene associated with autosomal recessive phenotype,40|Dosage sensitivity unlikely
         filterLabel.triploScore Triplosensitivity Score
 
     track clinGenCnv
     parent clinGenSuper off
     shortLabel ClinGen Copy Number Variants
     longLabel Clinical Genome Resource Copy Number Variants
     type bigBed 9 +
     itemRgb on
     visibility dense
     mergeSpannedItems off
     bigDataUrl /gbdb/$D/bbi/clinGen/clinGenCnv.bb
     mouseOverField _mouseOver
-    filter.size
     filterLabel.size Variant Size
     filterValues.variantType copy_number_loss|loss,copy_number_gain|gain
     filterLabel.variantType Copy Number Type (gain or loss)
     filterValues.clinicalInterpretation Pathogenic|pathogenic,Benign|benign
     filterLabel.clinicalInterpretation Benign or Pathogenic
     url https://www.ncbi.nlm.nih.gov/dbvar/variants/$$
     urlLabel NCBI DbVar:
     urls pubMed="https://pubmed.ncbi.nlm.nih.gov/$$/?from_single_result=$$&expanded_search_query=$$" clinGenId="https://dosage.clinicalgenome.org/clingen_region.cgi?id=$$&page=print"